visakhapatnam andhra pradesh analytical chemistry Jobs – 4 Open Jobs Today

Associate Manager - Quality Control
Pfizer —Visakhapatnam, Andhra Pradesh
- Full-time
- Laboratory experience
- Master's degree
- Continuous improvement
1d
Manager, Quality Assurance
Amneal Pharmaceuticals —Visakhapatnam, Andhra Pradesh
- Full-time
- Master's degree
- Bachelor's degree
- APIs
4d

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Associate Manager - Quality Assurance
Pfizer —Visakhapatnam, Andhra Pradesh
Good working knowledge of Microsoft Excel and Word. Ensure regulatory compliance with current Good Manufacturing Practices (GxP) and provide Quality Review and…
5d
Manager, Quality Assurance
Amneal Pharmaceuticals —Visakhapatnam, Andhra Pradesh
Support CMO, technology transfers, vendor qualification, and act as a quality interface for regulatory submissions and business requirements.
4d

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Associate Manager - Quality Control

Pfizer -
Visakhapatnam, Andhra Pradesh

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Job details

Full-time
1 day ago

Qualifications

Laboratory experience
Master's degree
Statistical analysis
Six Sigma
Quality assurance
Continuous improvement
Quality control
Data entry
Organizational skills
Pharmacy
Chemistry
Manufacturing
AI
Communication skills
Lean manufacturing

Full job description

Use Your Power for Purpose

Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard.

What You Will Achieve

In this role, you will:

Perform method transfers/ validations / method verifications to the complex analytical techniques
Interpret and evaluate data for accuracy, precision, trends, and potential cGMP impact, recommending appropriate corrective actions.
Ensure all documentation and quality records comply with Good Manufacturing Practices and Good Laboratory Practices and are filed according to existing policies.
Review and revise Standard Operating Procedures, analytical methods, and related documents to keep them current.
Conduct analyses on finished products, raw materials, and components, including data entry, review, and approval in a computerized database.
Contribute to the completion of complex projects, manage time effectively to meet targets, and develop plans for work activities within a team, while exercising judgment with reliance on supervisor and working under their direction.

Here Is What You Need (Minimum Requirements)

Master’s degree in chemistry/ pharmacy with 5-7 years of experience in Analytical Method Transfer / Validation)
Qualified in multiple analytical techniques (HPLC-with Empower, GC, IC, ICP-MS, Potentiometry, UV‑Vis, FTIR, Karl Fischer, and pH meters)
Demonstrated technical skills in method validation and testing
Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations
Conduct analytical method validation in accordance with ICH Q2 (R1/R2), USP, and EP standards, encompassing protocol preparation, execution, approval of validation summaries, and coordination with cross‑functional teams.
Conduct test method GAP assessments against USP, EP, BP, and JP requirements for New Product Introduction (NPI).
Execute and document analytical method verification and method transfer activities.
Demonstrate knowledge of ICH Q9 (Quality Risk Management) and apply risk‑based principles for identifying, assessing, controlling, communicating, and reviewing quality risks throughout the product lifecycle.
Perform identification, assay, purity, and related analytical tests using validated methods.
Monitor critical process parameters (CPPs) and critical quality attributes (CQAs).
Support process validation and troubleshooting activities; communicate analytical results promptly to Production and QA to ensure effective process control.
Manage working standards in compliance with established procedures.
Handle change control activities and ensure timely implementation and closure of related CAPA actions.
Knowledge of Good Manufacturing Practices and its application standards, processes, and policies.
Excellent organizational skills and strong ability to multi-task
Strong written and verbal communication skills
Proficiency with unique Quality Control instruments to meet accuracy specifications for sample management, retains management, interpretation, and evaluation

Bonus Points If You Have (Preferred Requirements)

Experience with laboratory work, particularly using analytical HPLC (High Pressure Liquid Chromatography),GC,IC, ICP-MS techniques
Proven track record in leading continuous improvement projects
Strong knowledge of lean manufacturing principles, six sigma methodologies, and statistical analysis
Strong problem-solving skills and attention to detail
Ability to manage multiple priorities and meet deadlines.
Excellent interpersonal skills and the ability to communicate effectively with colleagues at all levels
Adaptability and willingness to learn new techniques and procedures

Work Location Assignment: On Premise

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers.

Quality Assurance and Control

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