Cgmp Jobs in Malmo

Documentation Management like Issuance, Distribution, retrieval and destruction of documents i.e., SOPs, Formats, logbooks, Artwork, Lists, batch records, forms etc. and all other GMP documents. Preparation, review and revision of SOPs, Policies, Lists, SMF, Quality Manual etc More...

Direct Hire. 4555/hrFull time. El Segundo CA Responsibilities: The Senior Maintenance Technician will be responsible for the maintenance and repair of manufacturing and production equipment including calibration troubleshooting and preventative maintenance. This involves working wit More...

Temp Packaging Operator needs 2 years experienceTemp Packaging Operator requires:InventoryPackagingWarehouseProductionQualitycGMPTemp Packaging Operator duties: Setup operate and clear packaging line equipment and/or ancillary support equipment to meet efficiency expectations. Repleni More...

Perform project electrical and pneumatics hardware and PLC/HMI software design including test and validation activities on equipment and systems in accordance with applicable regulatory standards and to cGMP and GAMP 5 guidelines for the pharmaceutical industry. Liaise with associa More...

Biology Research Associate needs BS requires 35 years and MS requires 13 years of previous related experience. Biology Research Associate requires: Good working knowledge of cGMP regulations is required. BS or MS in a related science such as a Biology or Biochemistry is required S More...

Receive maintenance request for machines and distribute to technicians. Check breakdowns and follow up repairs for Utilities system. Follow up preventive maintenance of each Machine in the department and coordinate with the production operators. Issue spare parts PR for correctiv More...

Receive weekly production plan from Section Head. Supervise product preparation, compression, capsule filling, coating and inspection Issue and update SOP’s. Communicate with maintenance department about maintenance needs. Coordinate with validation department the required More...

Laboratory Support Technician II We are looking for a Lab Support Technician II to join our team. The Lab Support Technician II will ensure that all Buildings are cleaned and all equipment (tanks buckets and bottles) used in the manufacturing of SLI products are cleaned and stored pro More...

The QAOperations Specialist is responsible for quality assuranceoversight of manufacturing, testing and supply chain operationswith current GMP regulations, procedures and qualitysystems. JobDuties Provide shopfloor quality oversight ofall production, quality control and supply chain More...

Should be able to demonstrate strong understanding of USFDA/ MHRA/ EU or local guidelines. Responsible for setting strategy direction for the entire Quality Control & Microbiology Department and team. Conducts performance reviews for teams Development, review, revise and impl More...

We are hiring for QC AnalystDesignation Sr ExecutiveLocation NetherlandsQualifications Bachelors/Master of Science in Chemistry with Experience and working knowledge of CGMP regulations is required. Key Skills English language is required. To ensure the compliance with More...

Review Analytical documents Protocols and Reports of Stability Analytical Method Validation Analytical Method Verification and Analytical Method Transfer. Recording deviations and findings taking corrective and preventive actions defined and implemented in due time & trending of t More...

Please share your resumes at Job Role: Validation Engineer Contract: W2 Location: Newark CA Position Overview/Responsibilities: Ensure quality and compliance with established procedures and standards. Generate review and approve baselevel documents such as the Valid More...

POSITION RESPONSIBILITIES o Working knowledge of basic laboratory techniques for application in all aspects of Reagent Bead production o Assist in the development and maintenance of procedures used in Reagent Bead manufacturing o Reagent Formulation Lab equipment maintenance o Maintai More...

Qualifications B.S./M.S. degree in appropriate engineering/scientific field Minimum of 03 years postBachelors degree experience in a cGMP environment (e.g. Production Development Process Engineering Technical Services or related field) in pharmaceutical/ biotech industry P More...

Overview: We are seeking a Senior Automation Engineer with strong expertise in PLC DCS HMI and SCADA platforms. This role involves leading a team of engineers working directly with clients to identify requirements and delivering innovative automation solutions.Key Responsibilities:Dev More...

Strong understanding of USFDA/ MHRA/ EU or local guidelines Responsible for setting strategy direction for the entire Production Department and team. To enforce the batch manufacturing as per cGMP requirements in order to obtain high quality products. To achieve targeted producti More...

We are seeking a proactive Quality Assurance Coordinator to join our team. In this role you will support all Quality Systems to ensure quality manufacturing of products as defined by current Good Manufacturing Practices (GMP). You will assist other departments with quality and GMP iss More...

Job Description RESPONSIBILITIES Reports to the Facilities Manager interface with internal management and external auditors. Ensures activities on the Master Cleaning Schedule (MCS) are performed and documented Ensures that cGMP and Quality requirements are followed throu More...

JOB PURPOSE: To perform pharmaceutical microbiological procedures in compliance with FDA regulations and other regulatory/audit groups in order to ensure the accuracy of test results and raw data generated. KEY ACCOUNTABILITIES: Policies, Processes & Procedures: Follows a More...