Production Shift Supervisor – Late Shift Full Time NEW

The purpose of this position is to support the Laboratory as part of a team of supervisors, working closely with the Production Manager, Production Planner and other Departmental Managers.

The shift team lead role will direct the activities of team members and supervisors working within the production department, scheduling their work to meet production requirements and ensure an efficient and safe working environment.

Reports to: Production Manager

Location: 1 The Markham Centre, Station Road, Theale, Reading, Berkshire, RG7 4PE

Working Hours

Monday to Thursday: 1:45 PM – 10:30 PM

Friday: 1:45 PM – 6:15 PM

MAJOR JOB DUTIES AND RESPONSIBILITIES (List in order of importance)

• To assist with scheduling and overseeing workflow into the production areas in conjunction with the Laboratory Production Manager and Production Planner.
• Responsible for Workday administration for your team, including goal setting, holiday and absence approval.
• Set annual SMART goals for your team, run monthly reviews with all members of your team.
• To assist with managing day to day operations such as evaluation backlogs, system requirements and ensuring columns are submitted promptly.
• Lead by setting an example – motivate and inspire. Help keep team focused.
• Ensure working practices and all H&S protocols are always adhered to within lab – immediately report any concerns to PM and Safety Officer.
• Continues improvements around 6S.
• Provide encouragement to team members, identifying areas for new/further training – recommended suitability for production allocations.
• To assist with training when requested by manager.
• Answer team member questions and assist with problems such as method development or system troubleshooting and escalate issues which cannot be resolved by the team.
• Listen to team members feedback, resolve or escalate any issues/conflicts.
• Run regular 1-2-1 with all direct reports, formal and informal.
• Provide overall feedback to managers regarding work environment and procedures.
• Ongoing assessment of productivity and processing – regular feedback to LPM/Production Planner for discussion in weekly lab meetings.
• Coordinating with other Production Supervisors and covering for any supervisor absences where required.
• Locking up the site as well as any other tasks as required.
• Any other tasks as required

QUALIFICATIONS (Education/Training, Experience And Certifications)

• Good level of education, including English and Maths.
• Ability to use a range of other computer programs, including Excel, Word and Outlook

KNOWLEDGE, SKILLS, ABILITIES & COMPETENCIES (Those necessary to achieve conformity of products and services)

• SAP knowledge of production, inventory and material creation (desirable but not essential as full training will be given),
• Eexperience of supervising teams in a manufacturing environment
• Self-motivated, demonstrating initiative and results orientated
• Strives for continual improvement, demonstrates innovation and organisational agility
• Excellent communication skills, both verbal and written
• Ability to prioritize workload and multi-task
• High level of attention to detail
• Strong numerical skills with an understanding of volumetric weights/analysis
• A commitment to quality standards and the importance of following procedures
• An understanding of a HPLC/uHPLC column production environment (desirable but not essential as full training will be given)
• Ability to collect, analyse and implement improvements to TDM data

ENVIRONMENTAL WORKING CONDITIONS & PHYSICAL EFFORT (Under Typical Positions)

• This role is predominantly laboratory based, but will require some office administration
• Some degree of lifting and heavy work is likely with the daily moving of equipment, machinery and supplies

The above statements are intended to describe the general nature and level of work being performed by people assigned to this job. They are not intended to be an exhaustive list of all responsibilities, skills, efforts or working conditions associated with a job.

Disclaimer

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer.

Why Avantor?

Dare to go further in your career. Join our global team of 14,000+ associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science.

The work we do changes people’s lives for the better. It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his mom’s voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents, learn new skills and grow your career at Avantor.

We are committed to helping you on this journey through our diverse, equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor, dare to go further and see how the impact of your contributions set science in motion to create a better world. Apply today!

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We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state/province, or local law.

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