Seeking a 2nd and 3rd shift Assoc Scientist Chemistry for a 12 month assignment in Mount Vernon, IN.
All positions will be for 2nd and 3rd shift. General start times will be between 2-3pm for 2nd shift and 9-11pm for 3rd shift. 2nd shift is Monday - Friday and 3rd shift is Sunday - Thursday. Candidates may give shift perference but must be willing to work either shift.
Bachelors degree required.
The QC Analyst, Analytical Chemistry, performs and/or supports analytical chemistry testing on pharmaceutical raw materials, components, and/or finished product according to policy and procedures.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
1. Performs routine qualitative and quantitative analytical chemistry tests or audits on laboratory samples as assigned at a high level with a focus on quality and efficiency. Performs data review activities as required. Participates in QC team discussions and process improvement teams.2. Organizes daily work to ensure completion in a timely manner. Follow established methods, utilize approved laboratory techniques and perform routine calculations.3. Maintains current, complete, legible notebooks and laboratory records in compliance with good scientific and regulatory practices. Maintains adequate inventories of reagents, glassware, and other supplies.4. Writes and executes laboratory investigations for known laboratory errors and OOS results using Trackwise and/or other QC procedures.5. Executes laboratory processes in compliance with GMPs, site and corporate policies, standard operating procedures SOPs , and test methods. Immediately reports deviations that have the potential to compromise product quality.6. Maintains a safe work environment by following all Health Safety policies and procedures; immediately reports potential unsafe conditions to supervision.7. Maintains awareness of safety and emergency procedures and good laboratory practices as they apply to the work area.8. Utilizes Personal Protective Equipment PPE as necessary.
KNOWLEDGE / SKILLS:
1. BS/BA degree required; ideally in a scientific or technical discipline and/or relevant laboratory experience within a Pharmaceutical Quality Control Laboratory.2. Basic understanding of cGMPs and regulatory requirements as they relate to laboratory practices and manufacturing processes.3. Understanding of technical areas related to pharmaceutical manufacturing, analytical chemistry analyses, statistical methods, quality control, and quality assurance.4. Excellent interpersonal, verbal, and written communication skills with the ability to communicate with all levels of the organization.5. Ability to work in an action-oriented, fast-paced, and rapidly changing work environment.6. Ability to prioritize workload and manage multiple and varied tasks with enthusiasm.Possesses working knowledge of chemistry discipline. Interprets experiments and understands the range of working procedures in the team.
For immediate consideration please call 732-246-0215 or email to email@example.com