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  1. United States United States San Diego,
    Planet Pharma - Description: Title: Manufacturing/Validation Engineer I Company: Biopharmaceutical Duration: Permanent Location: San Diego, CA Description Entry-Level Manufacturing Engineer I will be responsible for supporting manufacturing and validation operations by working as an operator in all aspects of plasmid DNA manufacturing, including fermentation, centrifugation, lysis, and chromatographic processes and by applying engineering knowledge to troubleshoot problems and improve production capabilities. The Manufacturing Engineer will work with process validation and other associated groups to implement ... more
  2. United States United States Marlborough,
    Planet Pharma - Description: SUMMARY: One opening for 1st shift, one for 2nd shift. Candidates will need to start on the first shift for weeks for adequate training. Once they transition over to the 2nd shift, they will receive a 7% pay increase . 1. Testing of Liat™ Analyzer and sub-assemblies following documented procedures to assure conformance to specifications and standards. Completing documentation of work done and testing results as per procedures utilizing Good Documentation practices (GDP). 2. Ability to effectively troubleshoot routine test failures to the subassembly level, consulting with more e ... more
  3. Planet Pharma - Description: JOB SUMMARY: Responsible for development and implementation of various mass spectrometry-based methods for protein sequence confirmation, identification of modifications, identification of impurities and quantification of product variants to support process development, product characterization and similarity evaluations. Provide high quality data and actively participate in the activities of department cross-functional teams. Author standard operating procedures, test methods, method development reports, and aid in drafting CMC documents for regulatory submissions. ESSENTIAL FUNC ... more
  4. United States United States Raritan,
    Planet Pharma - Description: SENIOR SCIENTIST, Assay Development Job Description The Scientist position, Assay Development, will be working as part of a multi-disciplinary team, responsible for a compliant development of a new diagnostic medical device encompassing assay development and integration with the instrument and consumables. He/she will collaborate on refining assay requirements, developing the strategy for assay integration, and verification and validation activities. The candidate will be independently responsible for optimizing instrument related solution preparation, developing and qualifying te ... more
  5. United States United States Marlborough,
    Planet Pharma - Description: SUMMARY: Primary Responsibilities: Revision and Creation of Manufacturing Documents Release Testing of Reagent Tubes Instrument Final Release Testing Worker will be allocating 50% of their time as a reagent Technician and 50% as a Documentation specialist updating and writing new documents. Client would prefer someone from a production background who has maintained documentation. Requirements for the Documentation Specialist part is as below: 1. Writes Standard Operating Procedures (SOPs), Policies, Batch Production Records, Drawings, Data Collection Forms, Design History ... more
  6. United States United States Tucson,
    Planet Pharma - Description: Title: Engineering Tech II Location:Tucson, AZ Duration: 12 months The individual will be a member of Instrument Manufacturing supporting all production lines. As a skilled specialist, the individual will complete tasks in creative and effective ways and work on assignments requiring considerable judgment and initiative. The individual understands implications of the work and makes recommendations for solutions as well as determine methods and procedures on new assignments. ESSENTIAL FUNCTIONS: - Supports manufacturing technicians in the trouble shooting efforts as required. Is th ... more
  7. United States United States Houston,
    Planet Forward - Description: Description: Provide technical expertise for development, design and execution of instrument & electrical capital, expense and maintenance projects in a safe, profitable, timely and efficient manner. Education: BS in engineering is required. Qualifications Minimum of 5 years of experience in engineering and project management, preferably with at least 3 years exposure in a refinery/petrochemical-operating environment. Experience must be related to both instrument and electrical projects, including control system work. Supervisory skills are required, with the ability to com ... more
  8. United States United States Raleigh,
    Planet Pharma - Description: Quality Control Raw Materials Associate II Contract: 1 Year Location: Research Triangle Park, NC Client: Biotech The Quality Control Raw Materials Associate II will possess technical knowledge regarding Quality Control Raw Material methodologies. The position requires but is not limited to the following: demonstrated technical and analytical abilities, solid oral and written communication skills; ability to communicate with management and peers effectively and in a timely manner, effective organizational skills, developing or demonstrated problem solving skills, developing or demo ... more
  9. United States United States Butler,
    Air Products Careers - Description: Air Products and Chemicals, Inc. (NYSE:APD), a Fortune manufacturer of industrial gases and chemicals, is seeking an experienced Plant Operations Tech for its Butler, PA facility. To apply for this position, please visit the Air Products Career Center at . You can apply specifically to Job Req #BR. The Plant Operations Technician is responsible for controlling and monitoring a number of processes in the production of gaseous and liquid hydrogen and nitrogen. Daily activities include, but not limited to the following: - Actively participate in the basic safety process, sharin ... more
  10. United States United States California,
    Planet Pharma - Description: The Research Associate will participate in the early stage development of novel anti-infective compounds. This will include assay, potency and purity determinations by HPLC and GC using various type of detectors (MS, FID, UV and CLND). This position will aid in the identification of unknown impurities and degradants at various stages of synthetic pathways. Also, new analytical procedures and specifications will be documented as required. The candidate will interact with all the departments within the company. Essential Functions: · Assist in the quantitative evaluation of new com ... more