Global Calcium Pvt. Ltd., a leading pharmaceutical and API manufacturing company, has announced new career opportunities for qualified and experienced professionals in the Quality Control, Analytical Research & Development, and Production departments. Candidates with relevant pharmaceutical industry experience are invited to apply for these positions.

This recruitment drive offers excellent opportunities for chemistry and chemical engineering professionals seeking career growth in a reputed pharmaceutical organization.

About Global Calcium

Global Calcium is a well-established pharmaceutical company known for manufacturing Active Pharmaceutical Ingredients (APIs), mineral salts, and specialty pharmaceutical products. The company focuses on quality, innovation, regulatory compliance, and sustainable manufacturing practices.

Company Website: www.globalcalcium.com

Vacancy Details

Designation

Qualification

Experience

Officer – API QC

M.Sc. Chemistry

1–6 Years

Research Associate – Analytical R&D

M.Sc. Chemistry

3–6 Years

Officer – Production

B.Tech Chemical / B.Sc. Chemistry

0–4 Years

Eligibility Criteria

1. Officer – API Quality Control

Qualification: M.Sc. Chemistry

Experience: 1–6 Years

Key Responsibilities:

Analysis of API samples using analytical instruments.

Raw material, intermediate, and finished product testing.

Calibration and maintenance of laboratory instruments.

Preparation of analytical reports and documentation.

Compliance with GMP and regulatory guidelines.

2. Research Associate – Analytical R&D

Qualification: M.Sc. Chemistry

Experience: 3–6 Years

Key Responsibilities:

Analytical method development and validation.

Stability studies and impurity profiling.

Technology transfer support.

Investigation of Out of Specification (OOS) results.

Regulatory documentation preparation.

3. Officer – Production

Qualification: B.Tech Chemical / B.Sc. Chemistry

Experience: 0–4 Years

Key Responsibilities:

API manufacturing operations.

Process monitoring and batch execution.

Equipment operation and cleaning verification.

Documentation as per GMP requirements.

Ensuring safety and quality compliance.

Important Notes

Pharmaceutical experience is mandatory.

Male candidates are preferred.

Immediate joiners will be given preference.

Candidates should possess strong technical knowledge and documentation skills.

Freshers with relevant qualifications may apply for suitable Production positions.

How to Apply

Interested candidates can send their updated CV along with relevant documents to:

Email: gajapriya.k@globalcalciumpharma.com

For additional information, candidates may visit:

Website: www.globalcalcium.com

Career Email: career@globalcalciumpharma.com

Required Technical Skills

Candidates applying for these positions should have knowledge of:

For API QC

HPLC, GC, UV Spectrophotometer

Dissolution and assay testing

GMP and GLP compliance

Stability studies

Laboratory documentation

For Analytical R&D

Method development and validation

ICH Guidelines

Impurity profiling

Analytical troubleshooting

Regulatory documentation

For Production

API manufacturing processes

Batch manufacturing records

Process safety management

Equipment operation

GMP documentation practices

Technical FAQs

1. What analytical instruments are commonly used in API Quality Control?

API Quality Control laboratories typically use HPLC, Gas Chromatography (GC), UV-Visible Spectrophotometers, FTIR, Karl Fischer Titrators, and Dissolution Test Apparatus to ensure product quality and compliance.

2. What is analytical method validation in pharmaceutical R&D?

Analytical method validation is the process of proving that an analytical method consistently produces reliable and accurate results. Validation parameters include accuracy, precision, specificity, linearity, robustness, and detection limits as per ICH guidelines.

3. What is an OOS (Out of Specification) result?

An OOS result occurs when a test result falls outside the predefined acceptance criteria. It requires a thorough investigation to determine the root cause and implement corrective and preventive actions (CAPA).

4. Why is GMP important in pharmaceutical manufacturing?

Good Manufacturing Practices (GMP) ensure pharmaceutical products are consistently produced and controlled according to quality standards, minimizing risks related to contamination, mix-ups, and errors.

5. What is the role of Production Officers in API manufacturing?

Production Officers oversee manufacturing operations, monitor process parameters, maintain batch records, coordinate with quality teams, ensure compliance with SOPs, and support continuous process improvement.

Conclusion

Global Calcium’s latest recruitment drive presents an excellent opportunity for professionals in API Quality Control, Analytical R&D, and Production to join a reputed pharmaceutical organization. Candidates with the required qualifications, pharmaceutical experience, and technical expertise are encouraged to submit their applications at the earliest, especially immediate joiners seeking career advancement in the pharmaceutical industry.