Job Description
An amazing opportunity has arisen for a Raw Materials Research Specialist.
This role is part of our Analytical Research & Development department and this Specialist position will be a member of the Raw materials team. This role will specialise in ensuring material flows appropriately through the information management systems in use at site for material control. The role will be tasked with supporting material management for BARD at site.
The Specialist is expected to be a subject matter expert for material management flow and has a flavour for IT systems.
What you will do:
Bring energy, knowledge, innovation and leadership to carry out the following:
* Supporting raw material programs for all new biologics coming to site.
* Ensuring raw material testing proposed is appropriate, GMP, verified, tested, released as per the quality management system.
* Collaborate with a global network of scientists to streamline and platform scientific methods entering site.
* Propose Raw Material testing and specifications, Generation of Global test specifications, ensuring testing is qualified to GMP either internally or externally.
* Partner with the testing laboratories, Warehouse, supply chain, quality to ensure raw materials are released in accordance with GMP & internal procedures.
* Support of the Raw Material Systems Build & Maintenance on Comet & GLIMS .
* Author Raw Material Related Testing Investigations.
* Analyze and optimize current IT lab System business processes for the laboratories and support implementation activities of the technologies and methodologies.
* Works in accordance with applicable internal company regulations: safety, health and environmental protection.
What skills you will need:
In order to excel in this role, you will more than likely have:
* M.S in analytical chemistry/biochemistry or related field or B. S with a minimum of 3 years of experience in the Pharmaceutical Industry.
* GMP working experience and a working knowledge of regulatory requirements.
* Knowledge of Analytical Methodologies and sound scientific understanding with focus on liquid chromatography and IR spectroscopy.
* Team player with ability to support peer to peer coaching.
* Understanding of current manufacturing processes.
* Expertise in method validations and technology transfers.
* Initiate and support deviations, CAPAs, and, risk assessments, and change records as required.
* Author technical protocols and reports as required.
* Effective organizational and multi-tasking skills with strong oral and written communication skills.
* The successful candidate must be self-driven and confident to take ownership of sample management program & be able to collaborate in a fast-paced, integrated, multidisciplinary team environment.
As a company, we are committed to ‘Inventing for Life’ in all that we do. We keep the patient at the very heart of all that we do and strive to find solutions and treatments for some of the world’s most challenging healthcare needs.
We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment.
So, if you are ready to:
Invent solutions to meet unmet healthcare needs, Impact the future by driving one of the world’s leading healthcare companies, and inspire your team to reach their full potential and push the boundaries of science and technology, please apply today.
Current Employees apply HERE
Current Contingent Workers apply HERE
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
Regular
Relocation:
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements:
Not Applicable
Shift:
Valid Driving License:
Hazardous Material(s):
Job Posting End Date:
12/17/2024
*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Requisition ID:R325077
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