Senior QC Analyst

• JOB TITLE: Senior Analyst
• DEPARTMENT: Synergy Science
• LOCATION: Hull
• CONTRACT - The role is available for 12 months in the first instance with potential for extension/perm
• PAY - up to £28k (DOE)

Synergy are currently looking for a Senior Analyst to join their team working with a global health and wellbeing company based in Hull.



The Senior Analyst will work as part of a dynamic and high performing team providing stability analysis services across a portfolio of health and wellbeing products and projects.



The role will focus mainly on stability data generation in line with GMP/GLP standards, performing a variety of analytical techniques.



The role holder will be expected to demonstrate an understanding of method development, validation and transfer; QC/QA processes such as deviations, lab investigations, CAPA, and audit support; have experience of reviewing and approving data; and be able to train, coach and advise more junior members of the team.





PRINCIPAL ACCOUNTABILITIES:

• Perform sample assays on HPLCs and other instrumentation
• Analysis and trending of results
• Identify any out of specification / out of trend / unexpected results and to take the required remedial action
• Trouble shoot instrumentation issues
• Ensure samples are ordered correctly for stability storage and in accordance with SOPs
• Produce protocols for stability trials
• Pro-actively identify issues and take appropriate actions to address those issues
• Ensure compliance with all relevant Health and Safety systems and legislation applicable to your working environment
• Execute tasks according to regulatory, statutory, or client defined standards / requirements applicable to the service
• Train and advise new analysts in all aspects of the role
• Comply with all appropriate Synergy and Client defined Quality Management Systems, processes, and procedures, including the timely capture and recording of laboratory data
• Take an active role in investigations, deviations, change control and audits as required
• Take a lead role with regards to the continuous improvement of the wider team with respect to compliance, H&S, and audit readiness
• Meet / exceed the defined project KPI's & individual objectives
• Actively participate in Synergy training and performance review processes
• Develop and maintain excellent customer relationships, always ensuring that you act in a professional manner whilst performing your duties or whilst you are representing Synergy in any capacity
• Attend Customer meetings as required particular in the absence of the Project Manager
• Other duties as reasonably requested by the Synergy Project Manager

QUALIFICATIONS AND EXPERIENCE:

• Degree in a relevant scientific discipline such as Chemistry, Pharmaceutical or Biological Science, or equivalent professional experience
• Demonstrable experience of working as an Analyst or similar in a regulated environment (around 6 months - 1 year)
• knowledge or experience with GMP/other regulated environment
• Proven ability to train and coach others
• Quality mindset with attention to detail
• Results orientated, self-motivated with an ability to evaluate and take risks
• Excellent communication skills, including presentation skills
• Ability to work under pressure without compromising quality and delivery
• Strong intellectual curiosity with ability to think out of the box

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.