Quality analyst Work, Jobs in Keele, Sts (with Salaries)

Quality Control Analyst I
Teva —Salt
- Full-time
- Bachelor's degree
- Computer skills
- Communication skills
- Employee stock purchase plan
- Annual leave
1d
Aerosols Quality Analyst
Bespak —Holmes Chapel
- £25,000 - £27,000 a year
- Computer literacy
- English
- Quality control
- Free parking
- Annual leave
Quick apply

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Aerosols Quality Analyst
Bespak —Holmes Chapel
As a Aerosol Quality Analyst, you will be responsible for conducting testing and reporting laboratory activities to support the compliant and timely delivery of…
£25,000 - £27,000 a year
Quick apply

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Quality Control Analyst I

Teva -
Salt

Apply Now

Job details

Full-time
1 day ago

Benefits

Employee stock purchase plan
Annual leave
Employee assistance programme
Paid volunteer time
Life insurance

Qualifications

Non-conformance investigation
Analytical chemistry
Laboratory information management systems
ERP software
Bachelor's degree
Technical writing
Computer skills
SAP Manufacturing
Communication skills

Full job description

We Are Teva

We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.

Our Team, Your Impact

This position is responsible for performing testing and analysis of incoming materials, intermediates, finished products, swab samples, and other samples to support the commercial and development activities at the site in compliance with all regulatory requirements, company policies and procedures.

How You’ll Spend Your Day

All areas of responsibility listed below are essential to the satisfactory performance of this position by any incumbents with reasonable accommodation if necessary. Any non-essential functions are assumed to be included in other related duties or assignments.

Responsible for testing and analyzing incoming materials such as intermediates, finished products and swab samples.
Responsible for preparing, maintaining and reviewing thorough records, documentation on solutions, sample preparation and investigational/experimental samples.
Responsible for supporting laboratory investigations into Out of Specification/Out of Trend results or other laboratory events.
Responsible for performing revisions to documentation such as Standard Operating Procedures, Test Methods and Specifications.
Responsible for coordinating and sending materials for contract laboratory testing.
Responsible for compliance with DEA and site requirements regarding the handling, use and disposal of controlled substances.
Responsible for performing verification of compendial methods.
Responsible for providing training to other analysts on activities for which they have developed a level of expertise.
Responsible for performing peer review on documents which may also become a full-time role.
Responsible for assisting with activities associated with the stability program including sampling and statistical analyses.
Responsible for assisting with activities related to the sampling of incoming materials as needed.
Responsible for maintaining work areas and performing job functions in a safe and efficient manner in accordance with company policies and procedures, Good Manufacturing Practices (cGMP’s), Standard Operating Procedures (SOP’s) and Batch Record instructions.
Responsible for performing additional related duties as assigned.

Your Skills and Experience

Any equivalent combination of education, training and/or experience that fulfills the requirements of the position will be considered.

Education/Certification/Experience:

Requires a Bachelor’s degree, preferably in Chemistry or Microbiology, or equivalent education/experience with a minimum of 3 years relevant progressive experience in a Quality Control Laboratory environment.
Solid understanding of the principles of analytical chemistry as it applies to HPLC, GC, FTIR, UV-Vis and other general analytical techniques.
Requires working knowledge of cGMP, DEA and other applicable industry regulatory requirements as they relate to the production of pharmaceutical products and associated quality systems.
Prefer experience with Laboratory Information Management Systems (Labware LIMS and/or Empower preferred).

Also Good to Have

Skills/Knowledge/Abilities:

Computer proficiency with comprehensive working knowledge of MS Office products, Learning Management Systems (LMS), ERP systems such as SAP or Oracle and manufacturing/quality systems such as LIMS, Trackwise and Qdocs.
Ability to effectively document a process, explaining scientific and/or technical ideas in writing (technical writing skills).
Ability to communicate effectively with excellent written and oral communication skills.
Ability to interact positively and collaborate with co-workers, management and other internal stakeholders.
Self-directed with ability to organize and prioritize work.
Detail oriented with ability to identify errors and/or inconsistencies while performing tasks.

Problem Solving:

Works on problems of moderate scope where evaluation of contributing factors requires analysis of situation or data.
Exercises judgment within broadly defined practices and policies and selects methods and techniques for obtaining solutions.
Selects methods, techniques, and evaluation criteria for obtaining results.
Acts independently and proactively to recommend methods and procedures for problem resolution.

WORKING ENVIRONMENT

Exposure to fumes, odors, dusts, mists or gasses (for non-office).
Exposure to moving mechanical parts or moving equipment.
Exposure to low to moderate to loud noise levels.
May be required to wear personal protective equipment (PPE) as needed for assigned area and/or process (i.e. safety glasses, gloves, hearing protection, etc.).

How We’ll Take Care of You

At Teva, better health starts from within, and that includes you. From day one, you’ll be supported with benefits designed to help you thrive in and out of work. This includes generous annual leave, reward plans, flexible working schedules (dependent on role), access to tailored health support, and meaningful ways to give back to the community. When it comes to your career, you’ll be encouraged to explore, evolve, and shape your path. Twist, our one-stop shop for career development platform, gives you access to a wide range of possibilities, from learning programs and short-term projects to opportunities for internal growth. Here, you’ll be part of a culture that empowers you to reach your goals and prioritize your wellbeing every step of the way.

We offer a competitive benefits package, including:

Comprehensive Health Insurance: Medical, Dental, Vision, and Prescription coverage starting on the first day of employment, providing the employee enrolls.
Retirement Savings: 401(k) with employer match, up to 6% and an annual 3.75% Defined Contribution to the 401k plan.
Time Off: Paid Time Off including vacation, sick/safe time, caretaker time and holidays.
Life and Disability Protection: Company paid Life and Disability insurance.
Additional benefits include, but are not limited to, Employee Assistance Program, Employee Stock Purchase Plan, Tuition Assistance, Flexible Spending Accounts, Health Savings Account, Life Style Spending Account, Volunteer Time Off, Paid Parental Leave, if eligible , Family Building Benefits, Virtual Physical Therapy, Accident, Critical Illness and Hospital Indemnity Insurances, Identity Theft Protection, Legal Plan, Voluntary Life Insurance and Long Term Disability and more.

Already Working @Teva?

Make sure to apply through our internal career site on Twist—your one-stop shop for career development

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

Please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Request a reasonable accommodation by sending an email to [email protected] with the nature of your request and your contact information. Only inquiries concerning a request for a reasonable accommodation will be responded to from this email address.

Important notice to Employment Agencies - Please Read Carefully
Teva Pharmaceuticals USA does not accept unsolicited assistance from agencies 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.

Apply Now

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