The Quality Assurance Supervisor is responsible for ensuring timely and effective implementation of all Freshpet’s policies, procedures, and activities involved in assuring the quality of manufactured products.
Compensation
The salary range provided above is the range of the wages that we will pay for the listed position.
Responsibilities
Oversees the quality of products and processes, including raw materials and finished products
Ensures that products and processes comply with federal, state, and local regulations
Manages quality standards and policies, and measures performance against internal and external standards
Ensures that quality assurance programs and procedures are implemented correctly
Identifies, solves, and prevents problems that affect product quality
Requirements
Bachelor Degree of Science preferably in Food Science or related field (Meat Science, Biology, Microbiology, Food Microbiology, etc.)
Manages site regulatory compliance processes, including reporting, licensing support, Quality Technical Agreements, and documentation such as the Site Master File and Quality Manual.
Responsibilities
Lead and maintain site regulatory compliance programs to ensure adherence to applicable requirements, commitments, company standards, and current Good Manufacturing Practices.
Manage regulatory submissions, commercial data reporting, licensing activities, and maintenance of regulatory records supporting site operations.
Own and maintain the Site Master File and Quality Manual, ensuring documents remain current, accurate, and compliant.
Develop, review, negotiate, approve, and maintain Quality Technical Agreements with customers, suppliers, contract manufacturers, and business partners.
Support regulatory agency, customer, and pre-approval inspections through documentation preparation, coordination of responses, and follow-up activities.
Requirements
Bachelor’s degree in Chemistry
Bachelor’s degree in Biology
Bachelor’s degree in Pharmaceutical Sciences
Bachelor’s degree in Engineering
Nice to have: Managing Site Master Files and Quality Manuals
Maintain manufacturing equipment and lead continuous improvement initiatives in a pharmaceutical manufacturing setting.
Responsibilities
Maintain manufacturing equipment to ensure correct functionality, calibration compliance, and operation within validated process parameters.
Develop and guide the team toward achieving zero downtime, higher equipment reliability, and maximum availability through proactive maintenance strategies.
Lead continuous improvement initiatives such as LDM, TPM, debottlenecking, and resource optimization, while leveraging cross-site learnings for enhanced productivity and cost efficiency.
Prepare CAPEX proposals, conduct feasibility studies, secure approvals, and ensure timely execution of projects in compliance with regulatory and business requirements.
Manage OPEX budgeting, tracking, and monitoring, along with developing and reviewing KPIs to drive operational efficiency and cost control.
Requirements
Graduation in Mechanical, Electrical, Biotechnology Engineering or related field
Post Graduation in Engineering / MBA
Nice to have: 8+ years in engineering or plant maintenance roles
Nice to have: 5+ years as team lead managing Mechanical / Electrical / HVAC / Instrumentation / Operations / Engineering Projects in pharma manufacturing
Nice to have: Experience in cGMP, EHS, regulatory compliance and audit readiness in pharmaceutical manufacturing
Provide quality assurance and compliance expertise for Veterinary Medicine Research & Development (VMRD), including the design, execution, and transfer of new biological/biopharmaceutical products to ensure department and site objectives are achieved.
Responsibilities
Ensure VMRD production facilities and the transfer of newly developed and/or improved biological/biopharmaceutical products and processes comply with applicable USDA, EU, FDA, and Zoetis quality standards, as well as the regulatory requirements of destination countries.
Work in conjunction with VMRD Development Science & Technology (DST) colleagues on scale-up, technical transfers and coordination of regulatory issues.
Serve as QA consultant for development, clinical, and VICH batches/serials.
Support VMRD colleagues and initiatives by providing regulatory documents and manufacturing quality/compliance resources.
Review new product master batch records, manufacturing documents, and analytical documents for accuracy, completeness, and compliance with Outlines of Production/submissions, and provide QA approval.
Requirements
Bachelor's degree in biological or pharmaceutical sciences, engineering, or a related discipline (minimum 5 years experience)
Master's degree in biological or pharmaceutical sciences, engineering, or a related discipline (minimum 3 years experience)
Nice to have: Master's or PhD degree in a biological science or chemical/bioprocess engineering
Provide quality assurance and compliance expertise for Veterinary Medicine Research & Development (VMRD), including the design, execution, and transfer of new biological/biopharmaceutical products to ensure department and site objectives are achieved.
Responsibilities
Ensure VMRD production facilities and the transfer of newly developed and/or improved biological/biopharmaceutical products and processes comply with applicable USDA, EU, FDA, and Zoetis quality standards, as well as the regulatory requirements of destination countries.
Work in conjunction with VMRD Development Science & Technology (DST) colleagues on scale-up, technical transfers and coordination of regulatory issues.
Serve as QA consultant for development, clinical, and VICH batches/serials.
Support VMRD colleagues and initiatives by providing regulatory documents and manufacturing quality/compliance resources.
Review new product master batch records, manufacturing documents, and analytical documents for accuracy, completeness, and compliance with Outlines of Production/submissions, and provide QA approval.
Requirements
Bachelor's degree with 15 years' experience, or equivalent, in biological or pharmaceutical sciences, engineering, or related discipline.
Nice to have: Master's degree in a biological science or chemical/bioprocess engineering
Nice to have: PhD degree in a biological science or chemical/bioprocess engineering
Nice to have: Expert-level competency in the validation of processes, equipment, cleaning procedures, software, and computerized systems
Team Member - OSD Production (Granulation /Compression)
Dr Reddy's Laboratories Limited · Posted Nov 10, 2026
Production Operator responsible for setting up, calibrating, and operating manufacturing equipment for OSD products, ensuring compliance with GMP, GDP, and safety standards.
Responsibilities
Setting up and calibrating manufacturing machinery
Provide guidance, lead/co-lead projects for digital solutions, support complex investigations, and ensure product quality assurance and compliance with global regulatory agencies.
Compensation
The annual base salary for this position ranges from $82,700.00 to $137,900.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 10.0% of the base salary.
Responsibilities
Provide guidance, lead/co-lead projects for digital solutions
Routinely provide updates to the team and management on project milestones
Independently support complex investigations in cross-functional work areas, providing sound quality assurance judgment
Reviews and approves electronic record, protocols and reports
Authors, reviews, and approves SOPs
Requirements
High school diploma (or equivalent) with 8+ years of experience
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