ANKITKUMAR PATEL
Winnipeg,Canada
Summary
A highly dedicated and results-driven Production Chemist with proven experience in Oral solid dosage form, aseptic manufacturing and Sterile manufacturing in the Pharmaceutical Industry. Possesses detailed knowledge of the basic manufacturing of various dosage forms like Solids, small volume parenteral ( SVP) and large volume parenteral ( LVP). Skilled in regulatory compliance and quality assurance, including ICH, health Canada, EU and US guidelines. Strong problem-solving and critical thinking skills utilized to achieve efficient resolutions in complex production scenarios. Proven ability to foster a collaborative work environment, utilizing strong communication and interpersonal skills to inspire and motivate team members. Skilled in identifying strengths and areas for improvement and implementing tailored coaching strategies to enhance individual and team performance.
Overview
14
14
years of professional experience
Work History
Production Chemist
IVC Vita Health
Winnipeg
06.2024 - Current
- Conducted thorough cleaning and maintenance of encapsulation machines, tablet presses, and associated equipment to ensure optimal performance.
- Implemented interval testing procedures during production to uphold quality standards and meet product specifications.
- Utilized Labor Tracking computer systems and software to accurately record compression job orders and operations.
- Maintained precise documentation of all compression area activities, ensuring compliance with regulatory requirements.
- Operated tablet presses and encapsulation machines within established guidelines, prioritizing safety and equipment integrity.
- Maintained cleanliness and organization in the compression area to enhance efficiency and safety.
- Regularly inspected and maintained service equipment and tools according to manufacturers' guidelines.
- Adapted to varying production demands by performing additional tasks within the compression department as needed.
- Maintaining personal responsibility with Personal Protective Equipment (PPE)
- Demonstrated strict adherence to health and safety protocols, GMP standards, GDP and SOP policies.
- Responded promptly to task assignments from Manufacturing Manager or Supervisor, ensuring seamless operations.
Production Chemist
Genvion Corporation
Winnipeg, Canada
12.2019 - 10.2021
- Successfully executed batch processes in production facility following Standard Operating Procedures (SOPs), encompassing activities such as:
> Dispensing of raw material as per manufacturing batch record.Facilitating the solution making and transfer the raw material in blender as per batch record. Skillfully charging solution into designated blender. Conducting product transfer for drying , milling and sieving process while closely monitoring critical parameters. - Thoroughly completed essential production-related documentation, including accurate batch records and comprehensive logbooks.
- Continuously cleaned and organized work areas to remove safety hazards and maintain a minimum level of production errors.
- Followed standard operating procedures SOPs to ensure consistent product quality.
- Collected product samples at specified intervals.
- Conducted routine audits of safety procedures and personal protective equipment PPE compliance within manufacturing area.
- Communicated with management regarding production timelines, issues, and improvements.
- Trained new employees on essential job responsibilities, safety protocols, and company policies.
- Provided competent supervision to operators and effectively managed shift activities as required.
- Operated pharmaceutical manufacturing equipment ( Blender, Granulator, Spray dryer ) to produce high-quality products.
- Collaborated with team members to identify and resolve issues affecting productivity or quality.
- Ensured proper storage and handling of hazardous materials according to company guidelines and regulatory requirements.
- Documented operational data, maintaining records for temperatures, pressures, and, processing times.
- Reviewed batch records, logbooks, and other required documentation according to Good Manufacturing Practices GMP.
- Reviewed new SOPs or updates to existing SOPs as part of ongoing process improvement efforts.
- Participate in internal, external as well as Regulatory audits.
- Optimized new product development by coordinating cross-functional efforts between research and development, engineering and production teams.
- Loaded and unloaded trucks with Forklifts or pallet jacks (Certified forklift operator)
- Wrapped pallets securely in preparation for shipping and verify the documentation for shipping (Certificate of Analysis, Certificate of Manufacture and Certificate of Packaging).
- Perform the collection of samples of Raw materials and Packaging materials in the warehouse sampling room.
- Performs other related duties as assigned by Management.
Cashier
Mobil Gas Station
Winnipeg, Canada
12.2015 - 05.2021
- Greeted customers and answered any questions they had about the store's products and services.
- Issued receipts, refunds, credits or change due to customers.
- Stocked shelves with merchandise when needed.
- Answered customer inquiries regarding store policies and procedures.
- Balanced daily transactions on a computerized point-of-sale system.
Production Chemist
Marck Bioscience Ltd
Kheda, India
10.2010 - 06.2014
- Maintain cleanliness of the clean area as per SOP.
- Enter in to clean area as per the SOP and to check entry exit logbook of clean area.
- Raise the requisition of the disinfectant, IPA, Filter pads, cartridge filter and other miscellaneous item to concern department for clean area use.
- Check the availability of sterile garment and record the received and return quantity in logbook.
- Check and maintain the fogging activity at regular interval.
- Check the filter condition and gasket during the CIP /SIP activity.
- To assure status of CIP/SIP, Area cleaning, Batch Material Quantity and WFI release before commencing Batch Manufacturing.
- Check and maintain proper care during the handling, usage and storage of the cartridge filter.
- Executed timely and accurate production activities with use of batch record instructions, job aids and relevant SOPs.
- Prepared batch records, logbooks, and other required documentation according to Good Manufacturing Practices GMP.
- Cleaned and sanitized equipment regularly to maintain sterile work environment.
Education
Bachelor of Pharmacy - Pharmacy
North Maharashtra University
Shirpur , MH India06-2010
Diploma in Pharmacy - Pharmacy
Maharashtra State Board of Technical Education
Shirpur MH India06-2007
Skills
- Manufacturing and Operations Processes
- CGMP/GMP, GDP, and SDS
- Quality Assurance and Report Deviations
- Materials Handling and hazardous Materials Handling
- Clean room procedures
- EHS Rules and Regulations
- WHMIS
- Leadership
- Excellent English written and oral skills
- Multiple tasks and work well under pressure
- Microsoft Word, Excel, PowerPoint, Adobe Acrobat
Timeline
Production Chemist
IVC Vita Health
06.2024 - Current
Production Chemist
Genvion Corporation
12.2019 - 10.2021
Cashier
Mobil Gas Station
12.2015 - 05.2021
Production Chemist
Marck Bioscience Ltd
10.2010 - 06.2014
Bachelor of Pharmacy - Pharmacy
North Maharashtra University
Diploma in Pharmacy - Pharmacy
Maharashtra State Board of Technical Education
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