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Validation Engineer
Summary:
Validation Engineers to support the internal development and validation of a multi-dose preservative-free (MDPF) nozzle subsystem and any other miscellaneous project related deliverables as they arise. Scope Includes: Validation of new molding and assembly units Qualification of ISO7 clean rooms IntEmployment Type: Contract
Experience Level: Entry Level
Tags: Engineering Medical Device
Process Development Scientist
Summary:
Process Development Scientist provide direct support to the requirement, design, and characterization of inspection/packaging process, process optimization strategies and/or troubleshooting of operational issues in the operations. Apply advanced and diverse engineering principles to the design and iEmployment Type: Contract
Experience Level: Entry Level
Tags: Science Medical Device
Sr Engineer
Summary:
Sr Engineer with experience in Parenteral products, automatic and manual product inspection, vision system, device assembly and packaging.Employment Type: Contract
Experience Level: Entry Level
Tags: Science Medical Device
Quality Engineer
Summary:
Experienced Quality Engineer with a strong background in the Medical Devices industry. Proven ability to lead and execute commissioning and qualification activities in compliance with regulatory and quality standards. Skilled in conducting thorough investigations to identify root causes, ensure corrEmployment Type: Contract
Experience Level: Executive
Tags: Science Pharmaceuticals
CI/Process Specialist
Summary:
CI/Process Specialist responsible for developing the scope of work for different projects including but not limited to manufacturing areas. Work with functional areas to improve productivity, efficiency, and capacity. Provide engineering support to Lean Manufacturing activities. Responsibilities: MaEmployment Type: Contract
Experience Level: Executive
Tags: Science Medical Device
Laboratory Commissioning & Decommissioning
Summary:
The Laboratory Commissioning & Decommissioning Engineer will lead and execute technical projects involving the safe shutdown (decommissioning) and startup (commissioning) of laboratory facilities. This role is essential for ensuring smooth transitions of scientific infrastructure in compliance withEmployment Type: Contract
Experience Level: Executive
Tags: Science Pharmaceuticals
Validation Support Specialist
Summary:
Validation Support is responsible for providing support to the manufacturing areas related to process and product activities, giving assistance on new product introduction, product and process changes, maintenance of validation program, investigations and promoting continuous improvement of medicalEmployment Type: Contract
Experience Level: Entry Level
Tags: Science Medical Device
Validation Support Specialist
Summary:
Validation Support is responsible for providing support to the manufacturing areas related to process and product activities, giving assistance on new product introduction, product and process changes, maintenance of validation program, investigations and promoting continuous improvement of medicalEmployment Type: Contract
Experience Level: Entry Level
Tags: Science Medical Device
Validation Specialist
Summary:
Validation Specialist with a strong knowledge of injection molding processes to support the development, execution, and documentation of validation activities (Protocols, Tests, Reports). Familiarized with IQ, OQ and PQ validation phases for molds and equipment. IQ: Confirmation of Drawings (includiEmployment Type: Contract
Experience Level: Executive
Tags: Science Medical Device
Software Application Configuration Specialist
Summary:
Software Application Configuration Specialist with background in industries such as Medical Devices & Pharma. Responsibilities: Contribute to practice goals and continuous improvement initiatives technology. Engage in business process and/ or technology decision maker discussion related to integratiEmployment Type: Contract
Experience Level: Entry Level
Tags: Science Medical Device
Validation Engineer
Summary:
Validation Engineers to support the internal development and validation of a multi-dose preservative-free (MDPF) nozzle subsystem and any other miscellaneous project related deliverables as they arise. Scope Includes: Validation of new molding and assembly units Qualification of ISO7 clean rooms IntEmployment Type: Contract
Experience Level: Entry Level
Tags: Engineering Pharmaceuticals
CI/Process Specialist
Summary:
CI/Process Specialist responsible for developing the scope of work for different projects including but not limited to manufacturing areas. Work with functional areas to improve productivity, efficiency, and capacity. Provide engineering support to Lean Manufacturing activities. Responsibilities: MaEmployment Type: Contract
Experience Level: Entry Level
Tags: Engineering Pharmaceuticals
Quality Engineer
Summary:
Experienced Quality Engineer with a strong background in the Medical Devices industry, particularly in the transfer of equipment and products to new facilities. Proven ability to lead and execute commissioning and qualification activities in compliance with regulatory and quality standards. SkilledEmployment Type: Contract
Experience Level: Entry Level
Tags: Engineering Pharmaceuticals
QA Documentation Specialist
Summary:
Quality Assurance Specialist with strong expertise in GMP documentation and quality systems. This role blends traditional QA responsibilities with a focus on managing, reviewing, and controlling documentation to support compliance and operational excellence. Key Responsibilities: • Review, approve,Employment Type: Contract
Experience Level: Entry Level
Tags: Other Pharmaceuticals
Quality Investigations Specialist
Summary:
To perform chemistry laboratory investigations for pharma-biotech industry supporting the complaints system. Chemistry laboratory investigations management, including Root Cause Analysis. Lead and manage investigations, performing data analysis and trending of information to detect signals proactiveEmployment Type: Contract
Experience Level: Entry Level
Tags: Science Pharmaceuticals
Software Application Configuration Specialist
Summary:
Software Application Configuration Specialist to integrate their expertise in the implementation of TULIP System. Background in industries such as Medical Devices & Pharma. Responsibilities: Contribute to practice goals and continuous improvement initiatives technology. Engage in business process anEmployment Type: Contract
Experience Level: Entry Level
Validation Specialist
Summary:
Validation Specialist with experience in regulated industry. Knowledge and experience full validation life cycle. Process Validation Equipment Validation Reports ProtocolsEmployment Type: Contract
Experience Level: Entry Level
Tags: Science Medical Device
Sr. Engineer
Summary:
Sr Engineer with experience in Parenteral products, vision systems, device assembly and packaging.Employment Type: Contract
Experience Level: Executive
Tags: Engineering Pharmaceuticals
Specialist QA
Summary:
Quality Assurance Specialist to support quality operations in a GMP-regulated pharmaceutical environment. This role is responsible for ensuring compliance across manufacturing, packaging, and site systems, with a strong emphasis on documentation review, system approvals, and cross-functional collaboEmployment Type: Contract
Experience Level: Executive
Tags: Engineering Pharmaceuticals
Engineer
Summary:
We are seeking a skilled and innovative Engineer to join our dynamic team. The ideal candidate will have a background in engineering principles and practices, with experience in the purification process of protein, working with investigations, troubleshooting, process improvements and technical writEmployment Type: Contract
Experience Level: Executive
Tags: Engineering Pharmaceuticals