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Scientist - I (Assistant)
126 East Lincoln Avenue Rahway, NJ 07065 US
Job Description
Target Pay Rate: 30-36.14/hr **salary will be commensurate with experience
Job Description:
Device Product & Process Development (DPPD) Team focuses on the design, development, and commercialization of novel biologic/drug/vaccine-device combination products for safe and effective delivery to their intended sites of action. The DPPD Team oversees the development of the device constituent within our pipeline of combination products, spanning various therapeutic areas and routes of administration, including inhalation, implantation, and injection. The DPPD within our Company Research Labs is seeking a talented, self-motivated, and highly collaborative Scientist with knowledge of container closure integrity (CCI) technology and experience with test method development, testing, and method validation for various product images (vials, syringes, cartridges, and injectors) and secondary packaging. • The candidate will develop methods for our company’s combination product pipeline, inclusive of small molecule, biologics, and vaccine products. Principal Responsibilities • Develop, validate, and execute feasibility CCI studies for complex combination devices & delivery systems • Author technical reports and testing protocols • Review technical data to ensure compliance with cGMP standards • Collaborate with cross-functional teams to ensure successful tech transfer of analytical methods between QC labs
Qualifications:
Education/Work Experience Minimum Qualifications: • B.S./M.S in Mechanical Engineering, Biomedical Engineering, Industrial & Systems Engineering, Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or a related field/discipline with 0-1 years of relevant work experience in the pharmaceutical, biotechnology, or medical device industries Required Experience | Knowledge | Skills: • Relevant analytical execution, development, validation, and/or quality control (QC) for container closure integrity as it pertains to small molecule, biologics, and vaccine products. • Ability to learn new techniques, troubleshooting assays, author and review technical documents • Excellent organizational skills to manage multiple projects Preferred Experience | Knowledge | Skills: • Good Manufacturing Practices (cGMP) laboratory environment in large molecules (vaccines, biologics) with knowledge in container closure integrity methods. • Hands-on experience in CCIT method development, validation, and troubleshooting for injectable therapeutics. • Candidate should be familiar with the following CCIT technologies for this purpose: dye ingress, high voltage leak detection, vacuum and pressure decay, laser headspace analysis • Familiarity with compression/tensile testing (Instron, Zwick, Texture Analyzer), rheology (TA Instrument), metrology/non-destructive inspection (XRCT [Zeiss], Optical microscopy [Keyence], high-speed imaging) • Good technical, communication (oral and written), interpersonal, and teamwork skills. • Ability to effectively identify and communicate risks.
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Planet Pharma is an equal opportunity employer. It is our practice not to discriminate against any employee or applicant based on any criteria, condition or basis protected by laws or regulations in the locations where we do business. All qualified applicants are encouraged to apply. We celebrate diversity and are committed to providing an environment of mutual respect. We believe that diversity, equity and inclusion enable us to better meet our mission and values while serving our clients across the globe. If you have a disability or handicap and would like us to accommodate you in any reasonable way, please inform your recruiter, or contact us, so that we can discuss the appropriate alternatives available.
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