Brooks Steriscience Limited has announced exciting career opportunities for experienced pharmaceutical professionals at its Vadodara, Gujarat manufacturing facility. The company is recruiting candidates for multiple Quality Assurance (QA) departments, including QA-QMS, QA Validation, QA Documentation, and QA IPQA (API).

If you have relevant experience in the pharmaceutical industry and are looking to advance your career with a reputed organization, this is an excellent opportunity.

Company Details

Company Name: Brooks Steriscience Limited

Location:

Block No. 61/62, Village Manglej,

Nareshwar Road, Taluka Karjan,

District Vadodara, Gujarat – 391243

Job Openings

1. QA – QMS

Designation: Executive / Senior Executive

Qualification: B.Pharma / M.Pharma / M.Sc. (Chemistry)

Experience: 6–10 Years

2. QA – Validation

Designation: Officer / Senior Officer

Qualification: B.Pharma / M.Pharma / M.Sc. (Chemistry)

Experience: 3–5 Years

3. QA – Documentation

Designation: Officer

Qualification: B.Pharma / M.Pharma / M.Sc. (Chemistry)

Experience: 2–3 Years

4. QA – IPQA (API)

Designation: Officer

Qualification: B.Pharma / M.Pharma / M.Sc. (Chemistry)

Experience: 2–3 Years

Required Skills

Knowledge of cGMP and GDP practices

Experience in Quality Assurance systems

Documentation and SOP preparation

Validation protocols and reports

Investigation of deviations, CAPA, and change control

Regulatory compliance and audit readiness

Good communication and teamwork skills

How to Apply

Interested and eligible candidates can send their updated CV to:

Email: preeti.yadav@brookssteriscience.com

Only shortlisted candidates may be contacted by the company.

Technical FAQs

1. What are the key responsibilities of QA-QMS in the pharmaceutical industry?

QA-QMS professionals manage quality systems such as deviations, CAPA, change control, risk assessment, internal audits, SOP management, training compliance, and ensure adherence to cGMP and regulatory requirements.

2. What is the role of QA Validation?

QA Validation ensures that equipment, utilities, manufacturing processes, cleaning procedures, and analytical methods consistently produce quality products through qualification and validation activities.

3. What does an IPQA (API) Officer do?

An IPQA Officer performs in-process checks during API manufacturing, verifies batch records, monitors GMP compliance, conducts line clearance, and ensures manufacturing activities follow approved procedures.

4. Why is documentation important in pharmaceutical QA?

Proper documentation provides traceability, supports regulatory compliance, ensures data integrity, facilitates audits, and confirms that every manufacturing activity has been performed according to approved procedures.

5. Which regulatory guidelines should QA professionals be familiar with?

Candidates should have knowledge of cGMP, ICH Guidelines, Schedule M, US FDA, EU GMP, WHO GMP, ALCOA+ data integrity principles, deviation handling, CAPA, and change control systems.