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10.0 - 14.0 years
5 - 7 Lacs
pune
Work from Office
Role & responsibilities Independently handle the (QMS) change control, Risk Assessment, Deviation, Investigation, CAPA implementation, OOS, OOT, OOL Investigation, Process validation Protocol and report preparation, Internal and external audit compliance. Candidate having technical knowledge injectable manufacturing and water system. Knowledge of QMS Standards: Familiarity with ISO 9001, AS9100, or other relevant standards is essential. Internal & External Auditing: Ability to conduct audits, prepare reports, and ensure corrective actions are implemented. Process Improvement Tools: Proficiency in Six Sigma, Lean, and Total Quality Management (TQM) methodologies. Quality Core Tools: Expertise...
Posted 2 weeks ago
6.0 - 10.0 years
0 Lacs
pune, maharashtra
On-site
You will become a part of a quality-driven and compliance-focused production team responsible for manufacturing high-quality pharmaceutical products. Your role will contribute directly to ensuring uninterrupted production, regulatory compliance, and delivery of safe, effective medicines to patients. You will work in a GMP-regulated facility and collaborate closely with cross-functional teams like QA, Engineering, and Planning. Key Responsibilities: - Execute daily production activities (granulation, compression, coating, or packaging) as per approved batch manufacturing records (BMRs). - Ensure compliance with cGMP, safety, and regulatory guidelines during all production operations. - Superv...
Posted 3 weeks ago
2.0 - 7.0 years
2 - 6 Lacs
tada, sri city
Work from Office
Walk-in Drive | TIL Healthcare | Multiple Openings in Production, QA, Engineering & QC TIL Healthcare is a part of "Jhaver Group of Companies" having a turnover of USD 450mn whose core activities include Manufacturing, Marketing, Engineering, Construction and Trading like diversified businesses. Our plants are accredited approvals like EUGMP, TGAAustralia, UK MHRAetc. TIL manufactures Tablets, Liquids, Powders in Sachets, and Capsules and with well-known partners for several European companies. We are considered as Pioneers in Amino Acids in India and few known brands include ApetaminT/AstyminT/Astyfer/Neutrosec/Urelog/Peglec/HappenzT. Walk-in Interview Details: Date: Sunday, 28th September ...
Posted 1 month ago
5.0 - 10.0 years
0 Lacs
amritsar, punjab
On-site
As a QA Manager at Systacare, a trusted name in the pharmaceutical industry, your primary responsibility will be to ensure adherence to regulatory requirements and maintain the highest standards of compliance in injectable manufacturing. With a strong focus on innovation, compliance, and patient safety, Systacare is expanding its team and is seeking passionate professionals to join the organization. You will lead and manage the QA team to ensure compliance with cGMP, regulatory standards, and company SOPs. Your role will involve overseeing quality systems, including deviation management, change control, CAPA, OOS, and OOT investigations. It will be crucial for you to ensure quality assurance...
Posted 1 month ago
2.0 - 8.0 years
0 Lacs
maharashtra
On-site
You will be working as an Officer/Sr. Officer/Executive/Sr. Executive with 2-8 years of experience in injectable Manufacturing. Your role will involve following instructions and procedures outlined in the Entry-Exit SOP for Grade C and Grade B areas, as well as ensuring proper functioning and behavior in the aseptic area. You will be responsible for adhering to personnel hygiene practices within the factory premises, following Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) as per SOP guidelines, and monitoring temperature, relative humidity, and differential pressure. Additionally, you will be tasked with overseeing the handling of material movement in the producti...
Posted 3 months ago
5.0 - 9.0 years
0 Lacs
indore, madhya pradesh
On-site
The role we are offering is for a Block Head to lead a key production block within our injectable manufacturing facility. Your responsibilities will include overseeing end-to-end manufacturing operations, managing a team of production staff, driving process optimization, ensuring regulatory audit readiness, maintaining compliance with cGMP standards, implementing changes, overseeing equipment and maintenance, coordinating cross-functionally, and managing inventory and resources. You should have a degree in Pharmacy, Engineering, or a related field, along with proven experience in sterile/injectable manufacturing. Strong leadership and team management skills are required, as well as knowledge...
Posted 3 months ago
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