b pharm

Sr.Stat programmer clin pharmSyneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team...

**Company Description** P.A. College of Pharmacy (PACP) is a rapidly growing institute focused on pharmaceutical sciences and committed to delivering high-quality education and training. It is a professional educational venture of the P. A. Educational Trust (PAET) and is affiliated with Rajiv Gandhi University of Health Sciences, Bangalore, Karnataka. The...

DescriptionEssential Functions:Lead overall plant operations, including production, quality, engineering, warehousing, and support functionsEnsure compliance with GMP (Good Manufacturing Practices), regulatory requirements, and internal quality systemsDrive Strategic Planning and Execution to meet output, quality, cost, and delivery objectivesOversee...

Essential Functions: • Lead overall plant operations, including production, quality, engineering, warehousing, and support functions • Ensure compliance with GMP (Good Manufacturing Practices), regulatory requirements, and internal quality systems • Drive Strategic Planning and Execution to meet output, quality, cost, and delivery objectives •...

Description: This role is responsible for managing and executing analytical R&D documentation activities to ensure accuracy, consistency, and compliance with regulatory and data integrity requirements across drug substance and drug product development. The role supports preparation, review, and lifecycle management of analytical documents including...

DescriptionEssential Functions:Manage and coordinate technical writing activities for manufacturing SOPs, batch records, work instructions, and other GMP-critical documentsImplement and manage electronic document management systems to improve document accessibility and control efficiencyTranslate complex manufacturing processes and technical information into...

Job Description: This role is responsible for performing in-process, utility, environmental, and finished product microbiological testing in compliance with approved procedures, Good Manufacturing Practices (GMP), and applicable regulatory requirements. The incumbent evaluates microbiological test results for accuracy, precision, and compliance with...

DescriptionDescription:The role is responsible for ensuring day-to-day compliance with global GMP (Good Manufacturing Practices) during manufacturing, packing, and dispensing activities at the site. The role provides on-floor quality assurance support, ensuring operations are performed as per approved procedures, validated processes, and regulatory...

DescriptionPerform and review method validation of Assay, Dissolution, Related compound and Residual solvents etc. for new projects using instruments like HPLC,UV, IC ,GC,ICP MS and AAS etc. 2. Preparation of method validation/verification protocol (API and finish product) like HPLC, GC, IC, and AAS etc.3. Preparation of STPs and Specifications as per...

About Mettler Toledo METTLER TOLEDO is a leading global supplier of precision instruments and services. We are recognized as an innovation leader and our solutions are critical in key R&D, quality control, and manufacturing processes for customers in a wide range of industries including life sciences, food, and chemicals. We operate throughout the world with...

Qualifications: Highest Educational Background – B.Com, BBA, BBM, B. Pharm, B.Sc. Or any equivalent bachelor's degree Fresher or less than 1 year of work experience Graduated in the last 4 years (2021 or later) Provisional certificate or degree certificate Valid Aadhar number No prior apprenticeship program experience

Job Description:  Job DescriptionPurpose    To ensure the accurate dispensing of raw materials and/ or packaging materials to production as per Batch Manufacturing Records (BMR) in compliance with cGMP, GDP, requirements, maintaining data integrity and traceability. Activities include collection of materials from respective locations, line clearance,...

Maintain and follow the procedure as per SOP in day to day activity of warehouse. Receipt of materials, Physical verification and Preparation of Good Receipt Note in ERP systems and mail to concern user and purchase department. Affix status label (Quarantine) on all received materials and movement as per status updating. To update the record as per cGMP...

DescriptionKey Responsibilities:Prepare, execute, compile and review URS, DQ, IQ, OQ and PQ protocols and reports for sterile manufacturing equipment: vial and ampoule washing machines, depyrogenation tunnel, autoclaves, filling and sealing lines, capping machines, lyophilizers, RABS or isolators, CIP/SIP skids, and inspection machines.Participate in Factory...

DescriptionMaintain and follow the procedure as per SOP in day to day activity of warehouse.Receipt of materials, Physical verification and Preparation of Good Receipt Note in ERP systems and mail to concern user and purchase department.Affix status label (Quarantine) on all received materials and movement as per status updating.To update the record as per...

Description:The role is responsible for ensuring day-to-day compliance with global GMP (Good Manufacturing Practices) during manufacturing, packing, and dispensing activities at the site. The role provides on-floor quality assurance support, ensuring operations are performed as per approved procedures, validated processes, and regulatory expectations. The...

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to...

DescriptionDescription: Prepare and submit various regulatory applications, including Form 29, Form 11, Form 10, CT-11, CT-17, Forms 25 & 28, Chemist Approval, Written Confirmation, WHO-GMP Certification, Dual-Use NOC, RS-II, AC-II, MA-I & MA-II, Export Authorization and Import Authorization, and ensure timely follow-up and approvals from FDA, CDSCO,...

DescriptionJob Responsibility:Operation and cleaning of all Manufacturing equipments as per current version of respective SOPs.Maintaining the area and equipments in orderly manner as per cGMP requirements in a good state of repair and sanitized condition.Maintaining the tooling and change parts for all equipments at manufacturing.To follow safety rules.To...

DescriptionDescription:This role is responsible for conducting in-process and final product quality analyses and inspections in strict compliance with established standards and regulatory requirements within a global pharmaceutical manufacturing environment. The incumbent interprets and evaluates analytical results in terms of accuracy and precision against...