Halewood Laboratories
Website:
halewoodlabs.com
Job details:
Company Description Halewood Laboratories Private Limited, Unit-I, GIDC, Vatva, Ahmedabad is a global pharmaceutical manufacturer with over 40 years of experience, recognized as a leader in ORS and electrolyte solutions. The company operates state-of-the-art manufacturing facilities that comply with international standards, including WHO GMP, ISO, and ROW certifications. A strong focus on innovation allows Halewood to introduce 18–20 new, patented products annually, supported by a dedicated team of scientists, technocrats, and R&D experts. With a commitment to quality, integrity, and reliability, Halewood serves customers in more than 30 countries and continues to expand its presence in global healthcare markets.
Role Description The QA Executive and Assistant Manager role is a full-time, on-site position based in Gujarat, India. This role involves overseeing day-to-day quality assurance activities, including review and approval of batch manufacturing records, validation protocols, and standard operating procedures. Responsibilities include monitoring compliance with GMP and relevant regulatory requirements, coordinating internal and external audits, and implementing corrective and preventive actions. The role also requires collaboration with production, QC, and R&D teams to ensure consistent product quality, documentation accuracy, and continuous improvement of quality systems.
Qualifications
- Strong skills in Quality Assurance and Quality Management to oversee systems, documentation, and compliance.
- Well versed with handling and operation of Pharmacloud ERP system such as product master preparation, Formula master preparation, RM/PM code generation, Vendor updation, batch creation etc.
- Knowledge on equipment, instrument qualification, Process validation, Hold time study, Cleaning validation, Calibation calender preparation and maintenance, VMP and respective schedules preparation and updation.
- Proficiency in Quality Control to support testing, review of results, and release of products.
- Experience in Quality Auditing for conducting internal audits and supporting regulatory or customer inspections.
- Bachelor’s or Master’s degree in Pharmacy, Pharmaceutical Sciences, or a related field.
- Familiarity with GMP, PIC/S, ISO, and other relevant regulatory guidelines in pharmaceutical manufacturing.
- Strong analytical, documentation, and problem-solving abilities with attention to detail.
- Effective communication and teamwork skills, with the ability to coordinate across cross-functional teams.
- Prior experience in a pharmaceutical manufacturing QA function, preferably in liquids, powders, or similar dosage forms.
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