Executive / Sr. Executive - Quality Control

Company

SAVA Healthcare is amongst the fastest emerging pharmaceutical company in India with global reach to customers in Canada, Ukraine and the CIS, Asia, Latin America, Africa & FWA. With manufacturing units in Surendranagar, Malur and in near future in Indore holds various accreditations and produces wide variety of dosage forms across therapeutic categories.

Our GMP compliant, State of Art manufacturing facility for Tablet, Oral Dry Powder, Capsule, Nasal sprays, DPIs, Cream, Gel and Ointment formulations with dedicated manufacturing sections supported by In-House R&D Center, focuses on Formulation and Analytical Development with an annual turnover of more than 200 crores and manpower of 500+ employees engaged across locations.

Job Location

Surendranagar Plant, Gujarat

Job Summary

This position will be responsible for ensuring the quality and compliance of our manufacturing processes and products through rigorous validation protocols. This role is pivotal in maintaining our commitment to producing safe and effective pharmaceuticals.

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.

Qualifications

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.

Working Conditions

• Primarily office-based with regular interaction in laboratory and manufacturing environments.
• May require occasional travel for audits, training, and conferences.