Find Pharma, Biotech, Clinical Research & Medical Jobs on Bioksha
Description: This role is responsible for developing and optimizing pharmaceutical packaging systems by applying scientific and engineering principles to ensure product protection, stability, complian
We are looking for Upstream & Downstream Process Specialist for our Biosimilar manufacturing facility based out of Ahmedabad. Following are the Details of the Job . Education: Life science Graduate /
Department: Analytical Quality control Role: QC (Raw Material/Packing Material) Roles & Responsibilities Responsibiliti es: Sample management, including sample in/out, Entry/Exit of samples, Test samp
Key Responsibilities Compile, prepare, review, and submit high-quality US ANDA and EU marketing authorization applications, including original submissions and amendments, for MDI/DPI inhalation produc
Description: The role is responsible for ensuring effective day-to-day technical support to employees across a range of hardware and software systems. The role focuses on independently diagnosing comp
Description: The role is responsible for ensuring effective day-to-day technical support to employees across a range of hardware and software systems. The role focuses on independently diagnosing comp
Job Overview Job Title: Analytical Scientist Experience Level: 3 to 5 Years Department: Analytical Research & Development (ARD) Location: Ahmedabad No. of Positions: 20 Key Responsibilities Perform ph
Job Responsibility •To follow safety rules in the premises according to the company norms •Monitoring of DP, RH and temperature in aseptic processing area •To maintain the BMRs and other log books in
Description: This role supports the quality assurance function within a pharmaceutical manufacturing environment, contributing to the definition and specification of activities, processes, and standar
Description: The Human Resources Business Partner provides HR support to their respective client groups. The job requires the ability to forge strong business relationships with management at various
Required Competencies Strong understanding of formulation and process development of sterile injectable dosage forms for regulated markets. Hands-on experience and/or exposure to complex injectable sy
Description: This role is responsible for performing a variety of tasks related to the manufacturing of injectable pharmaceutical products within a regulated sterile manufacturing environment at a sen
To operate the necessary equipment such as cartridge washing, Filling, sealing, Autoclave, Auto Visual Inspection & batch manufacturing operation. To ensure compliance with cGMP. Maintain online docum
Description: 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-U
Assist Regional Compliance Lead in drafting / amending policies and procedures for the India Operations based on the changes in the regulatory environment Responsible for ensuring effective functionin
Description: This role is responsible for performing a diverse range of tasks related to the processing and assembly of pharmaceutical ingredients and finished products within a regulated sterile manu
Description: Responsible for implementing and maintaining Process Safety Management (PSM) systems to ensure safe plant operations. Conducts hazard identification studies, risk assessments, HAZOP revie
1 cGMP and compliance review in the GMP area as per cGMP guideline. 2 Machine and area clearance. 3 Sampling of blend, intermediate stages, AQL finished product, ANSI sample, reserve sample, stability
Essential Functions: Supervise QC laboratory operations and testing activities Review and interpret in-process and finished product analytical results Ensure compliance with GMP, GLP, and regulatory r
Description: The role is responsible for ensuring real-time compliance with global GMP (Good Manufacturing Practices) across manufacturing, packing, and dispensing operations. The role provides on-flo
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