chemist - process development / production.
waukegan , illinois
posted today
job detailssummary
$34 - $38 per hour
temp to perm
bachelor degree
category life, physical, and social science occupations
reference47743
job detailsjob summary:Randstad is the #1 HR talent engine in the world and we are sourcing for a Chemist in the northern suburbs of Chicago, IL. The ideal candidate will be working as part of a scientific team in a synthetic organic chemistry laboratory, with an emphasis on internal development of our clients High Purity Ingredient portfolio and execution of active pharmaceutical ingredient development and manufacturing projects. The Chemist must be able to work in a complex, fast paced environment with an ability to prioritize. Organization and attention to detail a must to maintain accuracy and quality of work. Must have good written and verbal communication skills. This is a direct hire position and it can start immediately.location: Waukegan, Illinoisjob type: Temporarysalary: $34 - 38 per hourwork hours: 7 to 3education: Bachelorsresponsibilities:
Produce cGMP high quality products that satisfy the Quality, Delivery, and Safety expectation of our biopharmaceutical and pharmaceutical customers
Participate in transfer in our cGMP high potency kilo lab and Pilot Plant manufacturing area
Perform production scale-up activities in support of research and development within our GMP API manufacturing areas
Execution of cGMP production as a production chemist of preclinical -commercial APIs scheduled within our cGMP kilo lab and pilot plant manufacturing suites
Conduct, as needed, laboratory chemistry experimentation in support of process development under the direction of a Senior Scientist from Process Development.
Support technology transfer to scale-up facility by providing shift technical coverage where applicable
Participate on project teams directed toward the development of active pharmaceutical ingredients and high purity ingredients
Ensure scientific integrity and quality of laboratory work they perform and review
Prepare and / or review technical reports and standard operating procedures
Communicate project status and problems encountered to management
Ensure accurate documentation and work in compliance with standard operating and safety procedures
Perform peer review of data for other staff members
Ensure adherence to site EH&S, GMP and general and laboratory and plant safety guidelines
Other duties as assigned
qualifications:
BA or BS in Chemistry, Chemical Engineering or applicable life science degree and 0-5+ years industrial laboratory experience related to process chemical development and/or small scale GMP manufacturing. Degreed scientist in an alternative life science field will be considered. Recent graduates with limited experience will be considered.
Willing to work flexible shift schedule to support manufacturing requirements
Familiarity with modern analytical methodologies utilized routinely in support of work, including HPLC and GC technique is a plus.
Compliance with cGMP regulations as applied to process development, optimization, production and engineering
Ability to exercise independent intellectual judgment based on specialized skills in the field of science
Organized and detail oriented for accuracy and quality of work in accordance with established procedures
Good written and verbal communications skills
Effective communication with manager and team members
Experience with the production of carbohydrates, amino acids and highly potent API's is desirable
Physical Requirements
Must have good hearing and sight - adequate for safety programs in a pharmaceutical manufacturing plant
Must be able to sit and/or stand for extended periods
Ability to work effectively under pressure to meet deadlines
Frequent sitting, standing, walking, climbing of stairs, use of computer monitor screen, talking, writing, listening
Must be able to lift 25 lbs. or occasionally lift up to 35 lbs.
Ability to wear proper safety equipment when working in the laboratory or plant
skills: Quality control, HPLC, SOP, Quality Assurance, Data Analysis, Analytical Chemistry, Biology, Chemistry, GLP (Good Laboratory Practice), Medicinal Chemistry, GMP (Good Manufacturing Practice), LIMS (Laboratory Information Management SystemEqual Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).Applications accepted on ongoing basis until filled.
Full-time