Global Calcium Pvt. Ltd. has announced a recruitment opportunity for the position of Quality Control Reviewer at its Unit-III facility in Hosur, Tamil Nadu. The company is looking for experienced professionals with a strong background in pharmaceutical quality control, analytical data review, and stability studies.

Candidates with an M.Sc. in Chemistry and 8–10 years of relevant experience in the pharmaceutical industry can apply for this opportunity.

Job Details

• Company Name: Global Calcium Pvt. Ltd.
• Department: Quality Control (QC)
• Position: QC Reviewer
• Qualification: M.Sc. Chemistry
• Experience: 8–10 years
• Pharma Experience: Mandatory
• Job Location: SIPCOT Industrial Complex, Phase I, Hosur, Tamil Nadu – 635126
• Application Email: ramya.d@globalcalciumpharma.in

Key Responsibilities

• Review and approve raw material, in-process, finished product, and stability data.
• Verify analytical methods, laboratory reports, and calibration records.
• Ensure data integrity and compliance with SOPs and regulatory requirements.
• Identify and communicate deviations, out-of-specification (OOS) results, and other quality concerns.
• Maintain accurate review records and quality documentation.
• Review and approve stability study data, protocols, and reports.
• Coordinate stability studies according to approved schedules and ICH guidelines.
• Monitor stability records, sample tracking, and related documentation.
• Review stability trends, investigate OOS results, and support shelf-life assessments.
• Ensure stability documentation complies with current Good Manufacturing Practice (cGMP) requirements.

How to Apply

Interested and eligible candidates can send their updated resumes to ramya.d@globalcalciumpharma.in. Applicants should highlight their pharmaceutical QC experience, analytical data review expertise, stability study experience, and knowledge of GMP documentation.

Candidates are advised to verify the vacancy details with the employer before applying.

Frequently Asked Questions (FAQs)

1. What is the qualification required for the Global Calcium QC Reviewer position?

Candidates must have an M.Sc. in Chemistry, along with 8–10 years of relevant experience. Pharmaceutical industry experience is mandatory.

2. What are the major responsibilities of a QC Reviewer?

The role involves reviewing analytical data, approving laboratory reports, verifying calibration records, ensuring data integrity, and maintaining compliance with quality procedures.

3. What is OOS in pharmaceutical quality control?

OOS stands for Out of Specification. It refers to a test result that falls outside the approved acceptance criteria. Such results must be investigated and documented according to established procedures.

4. Which guidelines are important for pharmaceutical stability studies?

ICH stability guidelines, including ICH Q1A(R2), provide guidance on stability testing and the evaluation of pharmaceutical products. Applicable regulatory requirements and approved company procedures must also be followed.

5. What is the importance of data integrity and cGMP in QC review?

Data integrity ensures that laboratory records are accurate, complete, consistent, and reliable. cGMP establishes requirements for maintaining product quality, proper documentation, and controlled manufacturing and testing processes.

Apply now: Send your updated resume to ramya.d@globalcalciumpharma.in for the Quality Control Reviewer opportunity at Global Calcium Pvt. Ltd., Hosur.