SEARCH

PRODUCTION TECHNICIAN Resume Example

Resume Score: 80%

Love this resume?Build Your Own Now
PRODUCTION TECHNICIAN
Professional Summary

Detail oriented professional with experience in both corporate and manufacturing environments. Versatile, Goal-oriented and excellent reputations with good planning abilities, project management and resolving problems.

Production Chemist and outstanding performer in Document as well as Compliance Specialist and Qualified Trainer within Amanta Healthcare Ltd. Recognized for inspiring management team members to excel and encouraging creative and positive work environments. Proven success in operational excellence, leadership and organizational development with profound understanding of elements of Pharmaceutical as well as Biotechnology business.

Skills
  • Verbal, Written, Management, Communication, and Documentation skills
  • Specification development and Investigation Specialist
  • Able to work in Multi-task and Team Environment but also as independent focusing on deadlines
  • Proven prioritization and excellent computer skills, including Excel, Word, PowerPoint, and Outlook
  • Ability to navigate organization with minimal direction, in support of completing tasks
  • Lean manufacturing processes along with good mechanical aptitude, Comprehensive and Retention skills
  • Knowledge of quality systems and Quality Control standards
  • Able to influence in proactive, objective and diplomatic way within all levels of company and work collaboratively
  • Troubleshooting and manual dexterity proficiency
  • Quality improvement leadership and prioritization
Work History
PRODUCTION TECHNICIAN03/2020 to Current
SANOFI PASTEUR – Swiftwater, PA

Safety: ●Participates in monthly safety meetings.

  • Works with safety team to ensure that resources required addressing safety issues are secured in timely manner and that effective resolutions are put into place and trained upon

Quality: ● FDA audit understanding and awareness.

  • Follows effective procedures to ensure production of safe and efficacious product. Adhere to all SOPs and cGMP's
  • Identifies areas of deficiency to management team and offers potential suggestions for improvements
  • Writes edits and reviews process documentation for completeness and Understands function of quality group
  • Participates in both deviation investigations when appropriate and implementation plans to ensure quality product

Delivery: ● Performs production in accordance with volume fluctuation, business need, and effective cGMP procedures.

  • Ensures all materials required for production are available prior to use
  • Works to prepare assigned areas for oncoming shifts and Works to complete quality documentation (BPR's, logbooks, etc.) accurately in timely manner
  • Completes sampling and corresponding documentation as required and Ensures completion of move tickets to ensure accurate inventory

Cost: ● Participates in all aspects of inventory management (SAP, cycle counting, ordering, LIMS, Deviation Trackwise, eDOC etc.).

  • Actively communicates improvement ideas, issues, concerns, etc. to team members along with providing solutions

Involvement: ● Involved in at least one cross functional teams where necessary to complete projects in effective and timely manner.

  • Completes at least one process training in new area whenever possible and Continues development by completing at least one developmental class annually
  • Works to become trained in all assigned training modules.
    All other duties as assigned
PRODUCTION CHEMIST12/2016 to 12/2017
AMANTA HEALTHCARE Ltd. – Kheda, India
  • Repaired, calibrated and safely operated all laboratory equipment as well as Resolved routine issues and escalated non-standard or critical issues to appropriate departments
  • Prepared and revised SOP's, BMR, BPR
  • Prepare and issue of daily and monthly formats and Performed Plant Induction
  • Prepare training calender of individuals employee and Impart Training to all new recruiters, staff and workers
  • To handle Change Controls, Deviations, CAPA, Market Complaints and Co-ordinate with QA department regarding any investigations and prepared reports
  • Performed complex data analysis, prepared reports complying with ICH guidelines, FDA, ISO, WHO, cGMP, internal regulations and Coordinated material
  • Faced audits like WHO, USFDA, MHRA, ISO, TGA and many more
  • Maintaining and Coordinating Record Retention Process of cGMP documents and document control through Production Floor Support
  • Prepare Validation plans, Protocols and Reports, Data Analysis and Validation Strategies in accordance with industry guidelines and SOP's
  • Check and maintain visual inspection of Product and Packing quality, as well as continuous monitoring rate of rejections
  • Communicates improvement ideas, issues, concerns to team members along with providing solutions and Resolves production issues related to area of work
  • Assures that operations are in compliance with Quality Systems, cGMP, CBER, WHO, EP and other regulatory bodies
  • Perform verification, crosscheck and signature in documents like BPR, Logbooks and other area documents
  • Knowledge of FDA, ICH guidelines, ISO and cGMP requirements, laboratory protocols, quality procedures and instruments like Handling Integrity Apparatus, Particle Count Machine
PHARMACIST08/2015 to 12/2016
SHETH H J MAHAGUJARAT MEDICAL STORE – Nadiad, India
  • Assisted patients in minimizing medical expenses by recommending generic alternative prescription medications
  • Ensured medications for content, accuracy and completeness of all drugs, packaging and labeling prescribed by medical and health professionals
  • Coordinated with both professionals and facilitated communication for absent information including drug strength, alternative medications and incomplete directions
  • Trained and supervised new pharmacy personnel's, technicians and supported staffs to provide excellent customer service on ongoing basis
  • Counseled patient on appropriate use of OTC as well as prescriptions medications
  • Ensure all pharmacy rules and regulations are being followed including supervision of pharmacy technicians and clerks on duty
  • Monitored ordering of pharmacy medication stock to maintain streamlined inventory and low overhead
  • Develops, implements and monitor policies and procedures involving drug formula, medications storage throughout facility, handling and control of all type of drugs
  • Integral member of continuous Quality Improvement Committee which evaluates workflow in order to reduce medication errors
  • Reviewed patient medication profiles and medical records to screen for appropriate drug selection, dosing, contraindications, side effects and therapeutic outcomes
  • Collaborated with physicians and other medical professionals to discuss and carry out orders as well as Managed pharmaceutical supply procurement and management processes
INTERNSHIP TRAINEE05/2015 to 06/2015
NABROS PHARMA Ltd. – Kheda, India
  • Was trained in various departments like Production, Quality Control, Quality Assurance and Packing
  • Learned more about overall pharmaceutical industry and its regulations including roles of each departments
  • Increased knowledge about importance of GMP, GLP and GDP practices
  • Learned to use various pharmaceutical as well as laboratory instruments
  • Detailed understanding of SUPAC guidelines
Education
Bachelor of Science: Pharmaceutical Sciences06/2015GUJARAT TECHNOLOGICAL UNIVERSITY- Ahmedabad

Broad Coursework in such as:

  • Instrumental and Pharmaceutical Analysis
  • Quality Systems
  • Pharmacology, Pathophysiology and Pharmacotherapeutics
  • Pharmaceutics and Dosage Form Design
  • Microbiology
  • Medicinal Chemistry
  • Organic and Inorganic Chemistry
  • Dispensing, Community, Hospital, Clinical and Forensic Pharmacy
  • Pharmaceutical Technology
  • Pharmacognosy
  • Unit Operations and Physical Pharmacy
  • Basic Computer Applications
  • Pharmaceutical Engineering
  • Elementary Mathematics and Biostatistics
  • Contributor Personality Development
International Exchange Program: Pharmacology And Medicinal Chemistry07/2014LAURENTIAN UNIVERSITY- Canada
  • Nominated to attain"International Experience Program"(IEP-2014) hosted by Laurentian University in Canada during my Bachelor's in Pharmacy.
  • Studied various prospects of Medicinal Chemistry and Pharmacology.
  • Research Paper term article on Evaluation of Anti-Inflammatory activity in Ethanolic Extract of Coriandrum Sativum L. using Carrageenan induced Paw Oedema in Albino rats.
  • Presentation on Designing and Development of Drug Molecule (Topic: Non-Zinc Chelating Inhibitor Drug Design) using Discovery Studios, PDB and Sci-Finder.
Certificate of Achievement : German Language2010Cambridge Institute- Ahmedabad
Build Your Own Now

DISCLAIMER

Resumes, and other information uploaded or provided by the user, are considered User Content governed by our Terms & Conditions. As such, it is not owned by us, and it is the user who retains ownership over such content.

Resume Overview

Companies Worked For:

  • SANOFI PASTEUR
  • AMANTA HEALTHCARE Ltd.
  • SHETH H J MAHAGUJARAT MEDICAL STORE
  • NABROS PHARMA Ltd.

School Attended

  • GUJARAT TECHNOLOGICAL UNIVERSITY
  • LAURENTIAN UNIVERSITY
  • Cambridge Institute

Job Titles Held:

  • PRODUCTION TECHNICIAN
  • PRODUCTION CHEMIST
  • PHARMACIST
  • INTERNSHIP TRAINEE

Degrees

  • Bachelor of Science : Pharmaceutical Sciences 06/2015
    International Exchange Program : Pharmacology And Medicinal Chemistry 07/2014
    Certificate of Achievement : German Language 2010

Similar Resumes

View All
Production-Technician-resume-sample

Production Technician

Man Power

Midkiff, West Virginia