Stark Pharma Jobs in United States

The GMP Operational Quality Senior Manager at Stark Pharma will oversee and ensure compliance with Good Manufacturing Practices (GMP) within manufacturing and quality assurance processes. · ...

The CMC Regulatory Affairs Associate will support regulatory submission activities with a strong focus on Chemistry, Manufacturing, and Controls. · Author, compile, and maintain Module 3 (CMC) sections for CTD and eCTD submissions. · ...

The CMC Regulatory Affairs Associate will support regulatory submission activities with a strong focus on Chemistry, Manufacturing and Controls. This role is hands-on and centered on authorizing reviewing managing Module section for CTD eCTD submissions within pharmaceutical envi ...

We're looking for a skilled CQV (Commissioning, Qualification, and Validation) Engineer to support a long-term pharmaceutical facility project. This is an onsite role requiring close coordination with construction and validation teams.Execute Facilities CQV activities... · ...

We are seeking an experienced CQV Automation Engineer with deep hands-on expertise in DeltaV systems. This role supports commissioning, qualification, and validation activities across instrumentation and control systems. · ...

The Senior Supply Planner will be responsible for end-to-end supply planning activities to ensure uninterrupted product availability while balancing inventory, service levels, and cost. · ...

The Quality Validation Engineer is responsible for executing equipment process and software validation activities in a regulated manufacturing environment. · ...

We are looking for a skilled Process Improvement Engineer to support our manufacturing operations in Columbus, Indiana. · ...

The Quality Assurance Senior Manager will lead and oversee quality operations supporting GMP manufacturing activities in Boston. This role is responsible for driving compliance and managing complex quality investigations. · ...

We are seeking an experienced Validation Engineer with strong EMPQ expertise to support a new facility startup. This role will focus on protocol development, execution, and documentation for facility and equipment qualification activities.Develop and execute EMPQ protocols includ ...

A leading life sciences company is seeking an experienced CQV Automation Engineer to support commissioning, qualification, and validation activities for DeltaV systems. This remote role requires over 10 years of experience in CQV processes, strong DeltaV expertise, and analytical ...

We are seeking an experienced CQV Engineer with deep hands-on expertise in DeltaV systems to support commissioning qualification validation activities across instrumentation control systems. · Develop execute CQV activities for DeltaV systems · Author detailed test scripts valida ...

We're looking for a skilled CQV (Commissioning, Qualification, and Validation) Engineer to support a long-term pharmaceutical facility project. · ...

The CMC Regulatory Affairs Associate will support regulatory submission activities with a strong focus on Chemistry, Manufacturing, and Controls. · Author, compile, and maintain Module 3 (CMC) sections for CTD and eCTD submissions · Support regulatory filings including INDs, NDAs ...

The GMP Operational Quality Senior Manager at Stark Pharma will oversee and ensure compliance with Good Manufacturing Practices within manufacturing and quality assurance processes. · Strong knowledge of GMP, Quality Assurance practices, and Validation processesExperience with re ...

Job Title: CQV Automation Engineer · Location: United States (Remote) · Experience: 10+ years · Work Model: Remote (with limited onsite travel) · Contract Type: Long-term contract (12 months+, extension likely) · Role Overview · We are seeking an experienced CQV Automation Engine ...

The Principal Mechanical Design Engineer will lead the design and development of complex mechanical and electro-mechanical subsystems for regulated medical device products.This role requires deep technical expertise, · strong design judgment, · and the ability to collaborate acro ...

The Process Validation Engineer is responsible for executing equipment, process, and software validation activities in a regulated manufacturing environment. · ...

We're looking for a skilled Equipment Validation Engineer/CQV (Commissioning, Qualification, and Validation) Engineer to support a long-term pharmaceutical facility project. · ...

The Lead Mechanical Engineer will lead the design and development of complex mechanical and electro-mechanical subsystems for regulated medical device products. · ...