SAVA Healthcare Hiring for Quality Control Jobs | Executive Roles | Apply Now
Looking for Quality Control Jobs in the pharmaceutical industry? SAVA Healthcare is hiring experienced professionals for Executive Jobs at its Surendranagar manufacturing facility in Gujarat. This opportunity is ideal for candidates with expertise in quality control, validation, GMP compliance, and analytical laboratory practices. If you’re passionate about ensuring pharmaceutical quality and regulatory excellence, this role offers an excellent platform for career growth.
About the Company:
SAVA Healthcare is one of India’s fastest-growing pharmaceutical companies with a strong global presence across Canada, Ukraine, CIS, Asia, Latin America, Africa, and FWA. The company operates GMP-compliant manufacturing facilities and an in-house R&D center focused on formulation and analytical development. Through these Executive Jobs, professionals can contribute to world-class pharmaceutical manufacturing while working in an environment that values innovation, quality, and continuous improvement.
Job Overview:
Quality Control Jobs are available at SAVA Healthcare for the position of Executive / Senior Executive – Quality Control. These Executive Jobs involve planning and executing validation activities, maintaining regulatory compliance, preparing technical documentation, supporting audits, and collaborating with quality assurance, manufacturing, and research teams. The selected candidates will play a key role in maintaining quality
standards while ensuring validation processes meet industry and regulatory requirements.Key Responsibilities:
- Validation Protocol Development: Develop and implement validation protocols (IQ/OQ/PQ) for equipment, systems, processes, and methods in the QC laboratory.
- Execution of Validation Activities: Conduct validation studies, including risk assessments, to ensure compliance with regulatory requirements and company standards.
- Documentation: Prepare and review validation documents, including protocols, reports, standard operating procedures (SOPs), and work instructions.
- Compliance: Ensure all validation activities comply with GMP, FDA, EMA, and other relevant regulatory guidelines.
- Audit Support: Support internal and external audits by providing validation documentation and responding to audit findings related to QC validation.
- Continuous Improvement: Identify opportunities for continuous improvement in validation processes and implement best practices.
- Training: Train QC staff on validation procedures and ensure adherence to validation standards and practices.
- Cross-functional Collaboration: Work closely with QA, manufacturing, and R&D teams to ensure successful validation activities and integration of new products/processes into production.
Eligibility Criteria:
- Education: Bachelor’s or Master’s degree in Chemistry, Pharmaceutical Sciences, or a related field.
- Experience: Minimum of 3 years of experience in QC validation within the pharmaceutical industry.
- Knowledge: In-depth knowledge of validation principles, GMP, FDA, EMA regulations, and industry standards.
- Technical Skills: Proficiency in analytical techniques and instrumentation, such as HPLC, GC, spectroscopy, and microbiological methods.
- Documentation Skills: Strong experience in writing and reviewing technical documents.
- Attention to Detail: High level of accuracy and attention to detail.
- Problem-solving: Excellent analytical and problem-solving skills.
- Communication: Strong verbal and written communication skills.
- Teamwork: Ability to work effectively in a team environment and collaborate with cross-functional teams.
Preferred Qualifications:
- Certification in Quality Assurance or Validation from a recognized institution.
- Experience with statistical analysis and validation software.
- Familiarity with Lean Six Sigma methodologies.
These Quality Control Jobs at SAVA Healthcare provide an excellent opportunity for professionals seeking rewarding Executive Jobs in the pharmaceutical industry. The role offers exposure to validation, regulatory compliance, analytical laboratories, and cross-functional collaboration within a modern manufacturing environment. Eligible candidates with relevant qualifications and experience are encouraged to apply and become part of a company committed to delivering high-quality pharmaceutical products.
Rasayanika is a career information portal and is not the recruiter for this position. All details are sourced from the official notification. Candidates should verify eligibility and deadlines on the official website before applying.
