Raw Materials Analyst (or Senior Analyst)

Raw Materials Analyst (or Senior Analyst) - West London

Overview:

The Raw Materials Analyst (or Senior Analyst) principal accountabilities are to support activities related to the management of Raw Materials at the London site, and to provide routine laboratory support tasks to other scientific staff.

Essential Functions:

• Manage Raw Materials throughout their lifecycle on the London site, under the oversight from the Quality Control and Analytical Chemistry Manager,
• Manage and participate in a range of Lab support activities. Line management responsibility for Support Services Assistant.
• Contribute to maintaining the Quality Management System (QMS) on documentation and activities related to raw material management, and support compliance activities in their area of responsibility.
• Management of Raw Materials on the London site, including but not limited to: ordering, receipt, liaising with suppliers and vendors, execution of Quality Control (QC) testing, inventory checks, disposal, management of raw material release documentation, including temporary filing on-site and preparation for archiving.
• Authoring of documentation required to support raw material management, e.g. Raw Material Specifications, technical reports, equipment related SOPs, risks assessments, etc.
• Performing investigations for Out Of Specification (OOS) results on raw material QC testing and support identification and implementation of CAPA (Corrective and Preventative Action).
• Conducting self-inspections (Quality and Safety) in their area of responsibility. Participating in external audits as required.
• Independently supporting analytical testing of raw material using a variety of techniques, including HPLC, GC, NMR, Melting Point, density, etc…Supporting training of other staff in these techniques as required.
• Maintaining analytical equipment in their area of responsibility, for routine use, and for preventative maintenance in conjunction with the Facilities Management Team.
• Coordinating and participating in laboratory support activities needed as part of operations, including but not limited to: glassware cleaning and storage, laboratories waste management, liquid nitrogen delivery at point of use across laboratories, performance checks and preventative maintenance for laboratory instruments (e.g. balances, water purifiers, pH meters, fridges/freezers), PPE (Personal Protective Equipment) inventory management and dispatch in relevant laboratories. Contribute to maintaining cleanliness and tidiness in GMP facilities.
• Other duties as assigned.

Qualifications:

• Education to BSc in a relevant scientific discipline, such as analytical chemistry or pharmaceuticals
• Minimum of 2-years practical laboratory experience (or 6-year for Senior Analyst position), in pharmaceutical settings or other related field.
• Good understanding of GMP, with prior experience working under GMP environment desirable
• Computer literate: competent in the use of a number of applications, including elements of the Microsoft Office suite, Internet and email software. Also conversant with industry-level database systems and analytical software.
• Good safety awareness.

Competitive Salary & Benefits:

Contributory Pension, Bonus, Private Medical Insurance, Life Assurance & Flexible Benefits options

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About us:

Headquartered in Boston, MA, Invicro was founded in 2008 with the mission of improving the role and function of imaging in translational drug discovery and development across all therapeutic areas. Today, Invicro’s multi-disciplinary team provides solutions to pharmaceutical and biotech companies across all stages of the drug development pipeline (Phase 0-IV), all imaging modalities and all therapeutic areas, including neurology, oncology, and systemic and rare diseases. Invicro’s quantitative biomarker services, advanced analytics and AI tools, and clinical operational services are backed by the company’s industry-leading software informatics platforms, VivoQuant® and iPACS®, as well as their pioneering IQ-Analytics Platform, which includes AmyloidIQ, TauIQ and DaTIQ.

Invicro is an Equal Opportunity Employer. We maintain a drug-free work environment. All qualified applicants will receive consideration for employment without regard to actual or perceived race (and traits historically associated with race, including, but not limited to hair texture and protective hairstyles such as braids, locks, and twists), color, creed, religion, citizenship status, sex or gender (including pregnancy, childbirth and related medical conditions), parental status, sexual orientation, gender identity, gender expression (including transgender status), national origin, ancestry, age, marital status or protected veteran status and will not be discriminated against on the basis of physical or mental disability, protected medical condition as defined by applicable state or local law, genetic information, political affiliation or any other characteristic protected by applicable federal, state, or local laws and ordinances.

Invicro does not accept unsolicited resumes from individual recruiters, third party recruiting agencies, outside recruiters or firms without an executed contract in place. We are not responsible for any fees related to resumes that are unsolicited or are received by Invicro. Such resumes will be deemed the sole property of Invicro and will be processed accordingly.

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