Global Calcium Hiring Quality Assurance

Global Calcium Hiring Quality Assurance
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B.Pharm/M.Sc QA Jobs Hosur API Plant

B.Pharm, M.Pharm, M.Sc candidates apply for QA roles at Global Calcium Hosur. 0–20 yrs experience. Apply now.

Global Calcium is hiring for multiple Quality Assurance (QA) positions at its pharmaceutical manufacturing facility in Hosur. This is a high-value opportunity for professionals looking for pharma QA jobs, regulatory compliance careers, API manufacturing quality roles, and GMP audit positions in a regulated pharmaceutical environment. Candidates with expertise in Quality Management Systems (QMS), CAPA, deviations, audit readiness, and pharmaceutical documentation can build strong long-term careers in one of the fastest-growing pharmaceutical quality domains.

Professionals with experience in USFDA, WHO-GMP, MHRA, and regulated manufacturing environments are especially in demand due to increasing global compliance requirements in pharmaceutical manufacturing.

Company Overview

Global Calcium is a well-established pharmaceutical and nutraceutical manufacturing company known for delivering quality-driven healthcare solutions. The company has built strong credibility in API and pharmaceutical manufacturing through its commitment to regulatory compliance, product quality, and operational excellence.

The Hosur manufacturing facility operates under strict pharmaceutical quality systems and international regulatory guidelines. Global Calcium focuses heavily on quality assurance processes, audit readiness, and continuous improvement, making it a strong workplace for professionals seeking careers in pharmaceutical QA and regulatory compliance.

Working in a regulated API manufacturing plant provides professionals with exposure to cGMP operations, pharmaceutical documentation systems, quality investigations, and international audit processes.

Job Role & Responsibilities

Global Calcium is hiring across multiple designation levels in the Quality Assurance department, ranging from Trainee Officer to Manager positions.

Key Responsibilities

Quality Management Systems (QMS)

  • Implement and maintain pharmaceutical Quality Management Systems
  • Ensure compliance with cGMP and global regulatory standards
  • Maintain audit readiness across departments

Deviations, CAPA & Change Control

  • Handle deviations, CAPA, OOS, OOT, and change control processes
  • Conduct root cause analysis and investigation activities
  • Prepare investigation reports and corrective action documentation

Documentation & Compliance

  • Prepare, review, and approve SOPs, BMR, BPR, protocols, and reports
  • Review analytical and manufacturing documentation
  • Ensure documentation compliance with regulatory standards

Audit & Regulatory Support

  • Conduct internal quality audits
  • Support external audits from USFDA, WHO, MHRA, and regulatory agencies
  • Coordinate with cross-functional teams during inspections and compliance reviews

Team Coordination & Training

  • Mentor junior QA team members for senior-level positions
  • Coordinate with manufacturing, QC, and regulatory departments
  • Support continuous quality improvement initiatives

These responsibilities are critical in maintaining pharmaceutical quality systems, ensuring patient safety, and supporting global healthcare compliance.

Eligibility / Qualifications

Qualification

  • B.Pharm
  • M.Pharm
  • M.Sc (Chemistry or relevant field)

Experience Requirement

  • 0 to 20 years depending on designation level

Industry Preference

  • Pharmaceutical / API Manufacturing
  • Regulated plant experience preferred

Relevant Courses

B.Pharm, M.Pharm Quality Assurance, M.Pharm Pharmaceutics, M.Sc Chemistry, M.Sc Pharmaceutical Chemistry, Regulatory Affairs Certification

Required Skills

  • Strong knowledge of pharmaceutical QA processes
  • Expertise in QMS, CAPA, deviations, OOS, and OOT
  • Regulatory compliance and audit handling knowledge
  • Documentation review and approval expertise
  • Good communication and cross-functional coordination skills
  • Attention to detail and GMP compliance understanding

Location & Salary

Work Location: Global Calcium Unit-III, Hosur

Salary: Competitive pharmaceutical QA salary package based on experience, designation, and regulatory expertise

Senior-level QA professionals with audit and regulatory compliance experience are among the highest-demand talent categories in pharmaceutical manufacturing.

Application Process

Interested candidates can share their updated profile to:

Email: ramakrishna.r@globalcalciumpharma.com

Important Notes

  • Immediate joiners are preferred
  • Candidates with short notice periods will receive preference

Applicants should ensure their resume highlights experience in pharmaceutical quality systems, audit handling, CAPA management, and GMP compliance.

Why This Opportunity Matters

Quality Assurance is one of the most critical and highest-paying functions in the pharmaceutical industry because it directly impacts product safety, regulatory approvals, and manufacturing compliance.

Professionals with expertise in QMS, CAPA, audit readiness, and pharmaceutical regulatory systems are highly valued in global pharmaceutical markets. Experience in regulated API manufacturing plants significantly improves career growth opportunities in multinational pharmaceutical companies.

Working in pharmaceutical QA also opens career paths into regulatory affairs, compliance leadership, validation management, and global quality operations.

Key Highlights

  • Company: Global Calcium
  • Department: Quality Assurance (QA)
  • Roles: Trainee Officer to Manager
  • Qualification: B.Pharm, M.Pharm, M.Sc
  • Experience: 0–20 Years
  • Industry: Pharmaceutical / API Manufacturing
  • Location: Hosur
  • Immediate Joiners Preferred

FAQs

Who can apply for Global Calcium QA jobs?

Candidates with B.Pharm, M.Pharm, or M.Sc qualifications and relevant QA experience can apply.

Is regulated plant experience required?

Regulated pharmaceutical or API plant experience is preferred.

What skills are preferred?

QMS, CAPA, deviations, OOS/OOT handling, audit readiness, and GMP documentation.

What designations are available?

Positions are open from Trainee Officer to Manager level.

How can I apply?

Candidates can apply by sending their updated CV to the official company email.

Summary Table

|———————————-|———————————-|
| Company | Global Calcium |
| Vacancies | Trainee Officer, Executive, Sr. Executive, Manager |
| Required Education | B.Pharm, M.Pharm, M.Sc |

Experience 0–20 Years
Global Calcium Hiring Quality Assurance
Global Calcium Hiring Quality Assurance

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