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Areas of Expertise
  • Quality control
  • Inventory management
  • Inventory control procedures
  • Materials accountability
  • Scheduling
  • DOT Training
  • Customer service-oriented
  • Manufacturing and warehouse procedures
  • Shipping and receiving
  • Rail transportation
  • HAZWOOPER Certificate 
  • Understanding of Distillation
  • Production scheduling
  • HAZMAT training & TWIC
  • Strong communication skills
  • Root cause analysis
  • Certified Forklift Operator
  • Strategic & Analytical thinker
  • Inventory tracking
  • Shipment consolidations planning
  • Decisive
  • Imports and exports
  • Cost reduction
  • Works well independently
Accomplishments
I've been proven capable to find common ground and solve problems. I am very cooperative, gained the trust of peers, and encourages collaboration. I cope well with change and I can shift gears. I've crossed training on multiple business groups. I can work with other business groups and back fill when needed. I base my decisions based on a mixture of analysis, wisdom, experience, and seek advice from my peers. I have been encouraged to pursue leadership developmental courses.
Experience
Kelly Services @ Dow Chemical Deer Park, Texas Site Logistics Rail Coordinator & Scheduler 08/2017 to Current
  • Review and identify constraints and/or restrictions that may impact the ability to fulfill requests
  • Communicate with site logistics contacts and carriers to inform them of scheduling plan exceptions
  • Initiate Management of Change process if changes to operating discipline are identified
  • Scheduling:Create and distribute scheduling plan to include all modes
  • Review the scheduling plan for completeness, manage changes, exceptions, and facilitate resolution of issues
  • Verify all shipment details for accuracy and completeness
  • Manage exceptions and extraordinary request made by the plant, customer, and customer service
  • Record necessary SAP system entries in a timely and efficient manner by completing activities like shipping - allocate product, perform goods issues, receipt process - return orders and raw materials
  • Bulk material transactions – Pipeline/Tank Material Transfers
DOW CHEMICAL Deer Park, Texas Site Logistics Rail Coordinator & Scheduler (Contractor) 10/2017 to 01/2018
  • Review and identify constraints and/or restrictions that may impact the ability to fulfill requests
  • Communicate with site logistics contacts and carriers to inform them of scheduling plan exceptions
  • Initiate Management of Change process if changes to operating discipline are identified
  • Scheduling:Create and distribute scheduling plan to include all modes
  • Review the scheduling plan for completeness, manage changes, exceptions, and facilitate resolution of issues
  • Verify all shipment details for accuracy and completeness
  • Manage exceptions and extraordinary request made by the plant, customer, and customer service
  • Record necessary SAP system entries in a timely and efficient manner by completing activities like shipping - allocate product, perform goods issues, receipt process - return orders and raw materials
  • Bulk material transactions – Pipeline/Tank Material Transfers
PHILLIPS 66 Sweeny, Texas TRAFFIC COORDINATOR (Contractor) 08/2017 to 09/2017
  • Collaborates with Phillips 66 and Chevron Phillips transactions in order to compile and process information such as bill of ladings, certificate of analysis and pick tickets
  • Checking inventories against truck and rail loads.
  • Issuing invoices and distributing them electronically
  • Communicating with Union Pacific to answer questions.Entering rail switch in UP site
  • Monitoring and maintaining rail/truck maintenance reports
  • Maintaining Transport Driver's Security and Safety records
  • Creating and maintaining Sulfur volumes for orders
  • Comparing load orders against SAP
ExxonMobil Baytown, TX Rail Logistics Coordinator (Contractor) 06/2015 to 08/2017
  • Coordinates the day-to-day movements and operations of rail fleet to gain optimal service and cost utilization for the Lubes and Specialties and Polyethylene business group
  • Processes billing for railcars that were loaded the day prior
  • Creates the schedule for the next day loads for future customer orders
  • Updates and maintains the transportation management systems, weekly and monthly statistics for management's stewardship
  • Coordinates with the refinery operations departments and quality team to optimize the supply chain, ensuring the most economic supplies are delivered to facilities in a timely fashion
  • Provide railcar order fulfillment for emergency situations, and oblige with internal and external customers
  • Works extensively in SAP GEMS, GOM, Stripes, Yardmaster, Rail Logix, and multiples spreadsheets and charts
  • Performs weekly reconciliation of railcar inventory in the facility to ensure continuous utilization and decrease demurrage 
Clean Harbors Environmental Laporte, Texas Receiving Chemist 02/2015 to 06/2015
  • Received lab pack containers and properly codes all chemicals for disposal processing
  • Performed consolidation of lab packs for final disposal as needed
  • Completed all paperwork associated with consolidation process
  • Performed lab pack bulking operations when needed and safely managed reactive materials for ultimate disposal
  • Performed lab pack systems operations through CHOICE or WIN. Specialized in Drum Receiving/Coding Operations, sampled all incoming drums and performs basic analysis of samples following prescribed procedures
  • Calibrated and utilized lab instrumentation required to run basic analysis. Completed all paperwork associated with analysis and drum sampling
  • Final coded routing and billing per CHI protocol and confirmed all drums were assigned properly for disposal process. Specialized in Shipping of Waste Materials
  • Assured materials were shipped prioritizing the inexpensive disposal outlets
  • Class B PPE required
Shell Chemical Deer Park, TX Material Coordinator (Contractor) 04/2014 to 02/2015
  • Effectively and efficiently manage the storage and movement of materials to facilitate the plants' reliability.
  • Process material movements, receipts, issues, and transfers in GSAP.
  • Maintain insurance for equipment such as pumps, valves, compressors, and rotors, spare parts such as bearings, mechanical seals, valves, gauges etc.
  • Generated weekly reports to optimize preservation and ensured trackability.
  • Assured all parts and equipment are inspected before issuing out to field or unit.
  • Operated propane operated forklift.
  • Class D PPE required.
ExxonMobil Beaumont, TX Inventory Control Analyst (Contractor) 02/2013 to 04/2014
  • Ensured timely and accurate information is maintained by lube plant personnel conducting business transactions for blending, packaging, shipping, receiving, and warehouse activities, in areas of inventory control, accounting, and costing.
  • Knowledgeable of all inventory matters on shift and communicated with the control room supervisors and operators in liaison of plant movements.
  • Coordinated with plant operations dealing with package filling, grease blending, batch oil blending, tank car loading, tank truck loading and unloading.
  • Generated gauging information for railcars
  • Used SAP, Stripes, GWM and GOM for inventory accounting and investigative purposes.
  • Delta V system and PI was also used for inventory investigation.
  • Performed monthly reconciliation of tank inventory 
Omega Protein Inc Cameron, LA Operator 01/2012 to 02/2013
  • Closely monitored four dehydration machines that vacuum dried finished products.
  • Monitored machine gauges, gathered samples for lab testing, and properly disposed of waste.
  • Recorded processing times and lab results.
  • Reported any malfunctions to area supervisor.
  • Maintained shop area, rotated drums, inspected motors, valves, and other machine parts.
  • Power washed work area after each shift.
  • Operated diesel powered forklift for moving heavy materials.
  • Worked in high noise area, worked around suspended loads, and offshore work.
  • Class C PPE required.
Education and Training
Associate of Science: Manufacturing Engineering / Process Technology May 2017 Lee College, Baytown, Texas, United States Process Technology / Manufacturing Engineering
Computer Skills
  • SAP Systems - GOM, GEMS, STRIPES, GWM
  • Borque Logistics System - Rail Trac & Yard Master
  • Sample Manager 
  • Microsoft Excel , Word, Powerpoint 

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Professional Summary

Detail-oriented Pharmacy Technician currently enrolled in Bachelor of Science program, interested in clinical pharmacology, pharmacy management and research. Certified Pharmacy Technician with three years' work at a leading national university chain and a small community pharmacy. Dedicated, hard-working, reliable and accurate professional who delivers courteous service at all times.

Chemistry professional involved in new material development and problem solving in new technology transfer. Skilled at identifying critical parameters in technology transfer.

Biochemistry with 4 years experience in quality control and quality assurance. Accomplished Chemist with a solid background in product invention, development and implementation. Thrives in a challenging environment while maintaining creative ingenuity. Analytical Research Chemist with exceptional problem solving and operational skills desires a position at a Chemistry lab.
Skills
  • MS Office Suite
  • Database Management
  • HIPAA Trained
  • Knowledge of Medicare and Medicaid
  • Accurate pharmaceutical calculations
  • Medication Inventory Management
  • Motivated self-starter
  • International Union of Pure and Applied Chemistry
  • International Union of Pure and Applied Chemistry
  • Society of Chemical Industry
  • Society of Chemical Industry
  • Specialization in colloid chemistry
Work History
07/2013 to Current
Manager USANA
  • Managed drug inventory levels, ordering medications and supplies for replenishment, verifying deliveries against purchase orders, and resolving any discrepancies.
  • Recruited, trained, and guided 3 pharmacy technicians, improving overall performance by 25%.
  • Implemented new guidelines and process workflow that minimized administrative errors from 2.3% to 0.1%.
  • Provided exceptional customer service that included additional information and education about medications, resulting in sales increase of $3K per month, while maintaining 83% in customer retention.
  • Eliminated paper-only tracking system, automating data management that saved 15 hours of manual data recording per week.
  • Dispensed medications according to written prescriptions with 100% accuracy and 29% more efficiency than other senior level pharmacists.
  • Verified patient data and billing information, discovering and resolving 20+ erroneous bills that occurred due to system error.
  • Analyzed organic and inorganic compounds to determine their chemical properties.





01/2016 to Current
Microbiology Open University Australia (Microbiolog Adelaide
  • Conducted basic and applied research on Microbiology.
  • Collected and analyzed biological data about relationships between organisms and their environment.
  • Programmed computers to store, process and analyze data.
  • Encouraged cooperative management strategies.
  • Interpreted research findings and summarized data into reports.
  • Extracted DNA and genotype samples using SNP technology.
  • Carried out quality control assessments for DNA analysis software.
  • Generated a dual thermal calibrator used in high resolution DNA melting.
  • Attended industry conferences to broaden knowledge.

01/2015 to Current
First Aid Ethiopian Orthodox Church Maribyrnong
  • Performed basic and advanced patient assessments.
  • Responded to dispatched emergency assignments quickly and safely.
  • Assessed patient condition through physical and verbal exams and by collecting information from others at the scene.
  • Administered infusion, medications and intubation.
  • Performed cardiac pacing and needle thoracotomy with great care and expertise.
  • Interpreted limited histories and used physical examinations to identify potential underlying critical issues.
  • Monitored patients for changes, and reviewed and revised plans accordingly.
  • Demonstrated high standards of performance, including teamwork, communication and compassion.

01/2015 to Current
Analytical Chemist Chemistry Charlies Sturt and Open University Australia
  • Operated and maintained analytical instruments such as FTIR, GC and Calorimeter.
  • Recorded test results using a variety of chemistry-specific software programs.
  • Conducted quality control tests and directed test procedures.
  • Organized lab test solutions, compounds and reagents.
  • Calibrated and troubleshot laboratory instruments.
  • Ordered chemicals for analysis and prepared reagents for analysis.
  • Accurately inventoried lab chemicals and supplies.
  • Created a rapid screening and testing factory to find acceptable materials.
  • Cultivated methods to screen metal content.


Affiliations
Bachelor of science with experience in pharmaceutical services *Adept at dispensing medications with accuracy and efficiency *Possess strong communication skills, consistently providing exceptional customer service *Increased overall productivity by implementing processes that improved workflow and reduced errors
Education
2013
Bachelor of Arts:
Swinburne University & Melbourne University -
2015
Associate of Applied Science: Biomedical
University of Adelaide Biomedical Science -
Accomplishments
Certifications

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Desirable Skills and Attributes
  • Plan and conduct research
  • Evaluate experimental methods
  • Make interpretative analyses of data
  • Critical thinking and analytical skill to solve problems
  • Ability to prioritize multiple tasks and projects
  • Self-disciplined and motivated to work independently 
  • Work well in a team setting or individually
Laboratory Skills

ANALYTICAL INSTRUMENTATION

LC/MS-MS Analytical System:

  • Agilent 1200 series LC system
  • Agilent G6410A Mass Spectrometer Triple Quadrupole with electrospray ionization (ESI)
  • MassHunter Workstation Acquisition Software
  • MassHunter Workstation Quantitative Analysis Program

GC/MS-MS Analytical System:

  • Agilent 7890A GC with Deans Switching System
  • Agilent 7693 autosampler
  • Agilent 7000 Mass Spectrometer Triple Quadrupole using negative chemical ionization (NCI)
  • MassHunter Workstation Acquisition Software
  • MassHunter Workstation Quantitative Analysis Program

GC/FPD Analytical System:

  • Agilent 6890 GC equipped with dual Flame Photometric Detectors (FPD)
  • Agilent 7683 autosampler

GC/ECD Analytical System:

  • Agilent 6890 GC equipped with dual Electron Capture Detectors (ECD)
  • Agilent 7683 autosampler

SAMPLE PREPARATION

  • Solid Phase Extraction (SPE)
  • Liquid Liquid Extraction
  • Accelerated Solvent Extraction (ASE)
  • Gel Permeation Chromatography (GPC)
  • Florisil Column

Perform sample analysis of various matrices for identification, confirmation and quantification of organic environmental contaminants using extraction methods and analytical instruments mentioned above.

Relevant Work Experience
Chemist (Range C), 08/2016 to 05/2017
California Department of Fish and Wildlife 2005 Nimbus Road, Rancho Cordova, CA 95670


Perform a variety of chemistry work within a laboratory.  Independently perform a variety of chemical analyses to detect low level pesticides and other contaminants in the environment.  Instrument set-up and sample extract analyses using laboratory instruments, LC/MS/MS.  Operate and maintain laboratory instrumentation.  Prepare standards and reagent solutions and samples for analysis.  Process data, review and write final reports.  Independently initiate and perform new methods set-up and validations.


Other laboratory experience includes gas chromatography with various detectors depending on the analytes of concern.

Chemist, 06/2001 to 08/2016
San Jose State University Research Foundation 2005 Nimbus Road, Rancho Cordova, CA 95670


Perform a variety of chemistry work within a laboratory.  Independently perform a variety of chemical analyses to detect low level pesticides and other contaminants in the environment.  Instrument set-up and sample extract analyses using laboratory instruments, LC/MS/MS.  Operate and maintain laboratory instrumentation.  Prepare standards and reagent solutions and samples for analysis.  Process data, review and write final reports.  Independently initiate and perform new methods set-up and validations.

Other laboratory experience includes gas chromatography with various detectors depending on the analytes of concern.

Education
Bachelor of Arts: Chemistry, 2001
California State University, Sacramento - 6000 J St, Sacramento, CA 95819

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PROFESSIONAL SUMMARY
  • A highly efficient, methodical and talented quality operations specialist with over a decade of experience in pharmaceuticals.
  • Thorough understanding of the essentials of safety, purity, efficacy, and quality.
  • Experience in production, quality management, & customer service.
  • Background of achievement in supporting all levels of management and working to set schedules & achieve targets.
TECHNICAL / RELEVANT SKILLS
  • Proficient in product quality, calibration, and qualification/validation/verification reports review
  • Able to handle root causes  & analyze their impact
  • ERP/QMS: JD Edwards, Qumas, Trackwise, LIMS
  • Flexible, methodical, & reliable
  • Responsible and able to finish tasks with accuracy & efficiency
  • Handle multi tasking and changing priority
PHARMACEUTICAL EXPERIENCE
Quality Assurance Supervisor 02/2018 to Current Pharmedium / Amerisource Bergen NJ
  • Guide, mentor, train, and educate employees (10-20 people) across shifts. Improve team performance by Identifying and evaluating employee's training requirements, giving cross functional training, & direct them to achieve cGMP compliance goals.
  • Manage new hire requisition, selection of candidate for an interview, conduct interview, and select good fit candidate.
  • Approve biweekly time, and time off requests. Make schedule according to the need and requirement of the company. Conduct training programs and quality meetings.
  • Collaborate with center management to complete audit responses, & ensuring that audits are closed within time frame.
  • Manage assigned compounding/manufacturing non-conformity events and/or deviations and customer product complaints for the site.
  • Evaluate corrective and preventive action responses and elevate issues to management as appropriate. Perform effectiveness checks on implemented corrective and preventive actions. 
  • Manage documentation changes for batch and system records via initiation of change control, escalate changes to compliance group, and train quality group upon approval of changes. 
  • Provide support, direction and coaching to employees for batch record review, batch release, visual inspection, stability, NOE/NCR, LIMS, SCAR, Label component approval, quarantine process,  documentation control process, sterility/endotoxin test sample submission to QC Lab, and internal audit of Aseptic technique. 
  • Coordinate and oversee environmental monitoring team for sampling, incubation, reading plates/media, deviation queries, and provide quality leadership for process improvement with right first time strategy. 
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  • Review and approve clean room Class ISO 5/7/8 documents, calibration reports, process validation reports, media qualification reports, Honeywell reports, and daily monitoring ISO 5 hood intelligence reports.
  • Execution of PPQ for software upgrade, and review it before submission to central IT compliance team.
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Quality Assurance Inspector III (Senior) 08/2015 to 02/2018 Amneal Pharmaceuticals NJ
  • Monitored and maintained quality and compliance targets of various generic products in a timely fashion.
  • Air sampling for new manufacturing areas validation.
  • Sampled and compiled the results of validation qualification of the Purified water system, USP.
  • Executed cleaning verification and validation processes for equipment.
  • Released packaging & raw materials for commercial production or ANDA batches, or R&D formulation development.
  • Released finished product for distribution center.
  • Compiled visual inspection data and performed visual inspection of retained finished products.
  • Tracked and retained raw materials and finished product samples, and submitted to QC according to all requirements.
  • Supported global stability management programs for ANDA submission with sample initiation to stability chamber, review  stability pullout schedule, and submit samples to QC/analytical R&D after each specified interval.
  • Reviewed and verified disposition of finished product and QC lab  waste.
  • Ensured that all QA records, data, and information are available to management.
  • Participated in execution of regulatory requirement for commercial products for labeling updates, CBE-30, and submission of samples specifications to FDA.
  • Released Batch after reviewing and compiling quality documents.
  • Reviewed and approved calibration reports of instruments, and validation reports of equipments.
  • Conducted on-site audit for repair, preventive maintenance, engineering floor drawing, calibration of equipment and utilities, escalate findings to management, and follow-up through change control.
  • Sampled ANDA, scale-up, pilot scale, technology transfer, and process validation batches.
  • Executed clinical trial for single blind / placebo study design with sampling, analysis schedule, and stability studies.
  • Composed the annual product review with data compilation, and annual product reports.
  • Assisted in customer complaint samples and Reference Listed Drug/Brand sample program.
Quality Assurance Associate 08/2013 to 08/2015 Heritage Pharma Labs NJ
  • Assisted in ANDA submission, SUPAC-IR, & validation batches And reviewed documentation.
  • Assisted in writing, editing, & implementing SOP as per guidelines of FDA 21 CFR 210, 211, and ICH Q7.
  • Performed validation/mapping studies of manufacturing, warehouse, & storage areas for their daily temperature, humidity, and air pressure with sensor monitoring system.
  • Reviewed equipment repair report for product quality risk and impact analysis.
  • Performed purified water USP system suitability test.
  • Initiated deviation process, and reviewed deviation investigation protocol.
  • Investigated probable root causes for non-conformance and reviewed CAPA and change control reports.
  • Audited product stability protocol at each interval during its life cycle to ensure consistency and compliance.
  • Issued manufacturing/packaging batch records, additional pages of MBR/PBR, and logbooks.
  • Created, issued, maintained, archived, and retrieved of logbooks. 
  • Approved cleaning validation protocol report to release equipments for the next step.
  • Organized & tracked training record, and updated it as necessary with ongoing training.
  • Reviewed Batch Manufacturing Record and protocol.
  • Calibrated micrometer, hardness tester, & friabilator.
  • Performed Acceptable Quality Level of tablet, coated tablets, capsules, & soft-gel capsules.
Quality and Regulatory Compliance Specialist 02/2012 to 07/2013 Vegan Herbs LLC NJ
  • Approved quality agreements, and marketing / advertising materials.
  • Executed internal audits throughout the distribution/ shipping facility.
  • Provided training for good distribution practices & preventive shipment errors.
  • Approved new product's label in order to fulfill FDA's nutritional regulatory compliance guidelines requirements.
Pharmacy Technician, Supervisor 02/2006 to 02/2012 Rite Aid and Community Pharmacy NJ & NY
  • Communicated & coordinated with insurance companies to ascertain patient benefits regarding brand or generic.
  • Provided patient care under the direct responsibility & supervision of a pharmacist, and explained OTC/non-prescription products to patients.
  • Maintained proper inventory levels, rotated stock and immediately complied with prescription drug recalls.
Quality Control Chemist 04/2003 to 06/2005 Hema Pharma India
  • Ordered supply for the laboratory.
  • Executed the Safe disposal of used chemicals.
  • Carried out finished product quality testing as per I.P. or B.P.
  • Performed analytical testing at various stages of bulk API manufacturing by GC, TLC, & pH.
Production Chemist 10/2001 to 12/2002 Nabros Pharma Ltd India
  • Managed manufacturing line with current GMP and monitored environmental factors.
  • Managed hold time of bulk product in quarantine area according to shipment priority.
  • Submitted purchase requisition to the management as per marketing/sales requirement. 
Education and Training
Post Graduate Diploma in Computer Science 2001 Sardar Patel University India
Bachelor in Pharmacy 1998 KLE's College of Pharmacy India
Certified Quality Auditor 2017 ASQ - Milwaukee USA
Drug Development Certificate (Expected completion in Dec-2018) 2018 Temple University USA