Quality Assurance Specialist
7 days ago
Company Description
Msea Pharmaceuticals is located in Ponta Sahib ( manufacturing unit under the Daksh Group). We are committed to providing high-quality medicines to individuals worldwide, with a focus on making healthcare accessible and affordable. Our diverse portfolio of medicines covers various therapeutic areas. We prioritize quality and adhere to stringent regulatory standards to ensure the safety and effectiveness of our products.
We are looking for a highly experienced and dedicated professional for the role of
QA Head & Documentation
at
Panchkula, Haryana
. This is a senior leadership opportunity for professionals with
20+ years of experience
in
pharmaceutical quality assurance, documentation, and compliance
.
Position Details
- Designation:
QA Head & Documentation - Experience:
Minimum 20 years in Pharma (Formulations / Manufacturing / Exports) - Location:
Panchkula, Haryana - Industry:
Pharmaceuticals – Domestic & Export
Key Responsibilities
As the
QA Head & Documentation
, you will be responsible for ensuring the highest standards of quality, compliance, and operational excellence across our manufacturing and export units.
- Leadership & Oversight
- Oversee the
entire manufacturing unit's quality assurance activities
, ensuring compliance with
WHO-GMP and other global regulatory standards
. - Monitor day-to-day operations, ensuring smooth functioning of the QA systems.
- Documentation & Compliance
- Supervise all
manufacturing unit documentation, export documentation, and compliance reports
. - Maintain and review
batch manufacturing records (BMRs), standard operating procedures (SOPs), and export regulatory documentation
. - Ensure timely submission and accuracy of
daily QA reports and audit records
. - Audits & Regulatory Affairs
- Lead
internal and external audits
with regulatory authorities. - Ensure the unit is always prepared for inspections from
domestic and international agencies
. - Training & Development
- Develop and implement
training protocols for QA staff, production team, and recruits
. - Regularly conduct
quality training sessions
to maintain a compliance culture across departments. - Reporting & Review
- Oversee
daily quality assurance reports, deviations, and CAPA (Corrective & Preventive Actions)
. - Present quality and compliance updates to senior management.
Candidate Profile
- Minimum
20 years of experience
in
Quality Assurance, Documentation, and Regulatory Compliance
within the pharmaceutical industry. - Strong knowledge of
domestic and export regulatory frameworks
. - Proven ability to
lead large QA teams
and handle multi-unit operations. - Hands-on expertise in
manufacturing documentation, audits, and training protocols
. - Excellent communication, leadership, and decision-making skills.
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