At a Glance
- Tasks: Lead quality assurance efforts and ensure timely batch releases in a dynamic pharmaceutical environment.
- Company: Join Hikma Pharmaceuticals, a trusted leader in essential medicines worldwide.
- Benefits: Enjoy competitive salary, generous PTO, health benefits, and career growth opportunities.
- Other info: Be part of a company prioritising safety, quality, and employee wellbeing.
- Why this job: Make a real impact on patient health while advancing your career in a supportive team.
- Qualifications: Experience in Quality Assurance or production, with supervisory skills preferred.
The predicted salary is between 66600 - 133750 £ per year.
Location: Bedford, Ohio
Job Type: Full-time
Req ID: 11286
About Us: As a developer, manufacturer, and supplier of essential medicines, Hikma Pharmaceuticals USA Inc. and its affiliates’ purpose is to put better health within reach, every day for millions of patients around the world. We are a trusted, reliable partner and dependable source of over 760 high-quality generic, specialty and branded pharmaceutical products that hospitals, physicians and pharmacists need to treat their patients across North America, the Middle East, North Africa and Europe. Through our global footprint of 30+ manufacturing plants, 8+ R&D centers, and 9,000+ empowered employees, we are committed to making high-quality medicines accessible to the people who need them.
JOB PURPOSE: The Quality Assurance Supervisor works closely with multiple departments to ensure batches are dispositioned appropriately and released in a timely manner. The Quality Assurance Supervisor will also manage the incoming inspection and retain program. This position is responsible for the timely review of all documentation associated with the batch record, and assisting with actions associated with environmental issues, placing materials/batches on hold, and communicating the status of production batches.
KEY ACCOUNTABILITIES:
- Regular and predictable onsite attendance and punctuality.
- Lead ongoing daily departmental activities for areas of direct responsibility including supervision of assigned personnel, and when required assist other Quality areas in the successful performance of these activities.
- Manage activities of self and direct reports in achieving defined quality goals in an efficient, accurate and timely manner.
- Be directly involved in and where appropriate lead multiple process/product improvement projects which may include Lean Manufacturing or other focus groups, design of experiments, validation protocols.
- Lead internal and external audit ready status efforts for assigned areas and assist other areas within the facility in understanding FDA and company quality requirements.
- Maintain a high level of expertise in current regulatory requirements and serve as a plant resource for compliance to these requirements.
- Must be recognized by all levels of the facility as an expert in their area and be able to demonstrate leadership ability.
- Work with operations personnel to identify and develop corrective actions for deviations.
QUALIFICATIONS
Minimum: Associate’s degree in science or related field with 7 to 10 years applicable experience.
Preferred: Bachelor’s degree in science or related field with 5 to 7 years applicable experience.
EXPERIENCE:
Minimum: 3 years’ experience in the pharmaceutical industry, in the field of Quality Assurance or production.
Preferred: Supervisory Experience.
Compensation: Base Salary: to $66,600 to $133,750 annually. The compensation for this position will be determined during the interview process and will vary based on multiple factors, including, but not limited to, work location, prior experience and job-related knowledge, relevant skills and expertise, current business needs, and market factors.
What We Offer:
- Annual performance bonus, commission, and share potential.
- Auto enrollment in a Hikma-sponsored 401(k) program at a pre-tax contribution rate of 3% of eligible pay. Hikma will match 100% of the first 6% of eligible pay that you contribute.
- A generous paid time off (PTO) bank starting with 20 days (prorated based on hire date). Additional days granted upon reaching work milestone anniversaries.
- 3 personal days (prorated based on hire date).
- 11 company paid holidays.
- Comprehensive benefits including health, dental, vision, mental health, disability, life insurance, prescription drug coverage, and a variety of voluntary benefits.
- Employee discount program.
- Wellbeing rewards program.
- Safety and Quality is a top organizational priority.
- Career advancement and growth opportunities.
- Tuition reimbursement.
- Paid maternity and parental leave.
*Eligibility requirements apply to some benefits and depend on the job classification, role, and length of employment. Benefits are subject to change as well as specific plan or program terms.
Equal Opportunity Employer: Hikma Pharmaceuticals USA Inc. is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status, or other characteristics protected by law.
Supervisor, Quality Assurance in Bedford employer: Hikma Pharmaceuticals USA Inc.
Hikma Pharmaceuticals USA Inc. is an exceptional employer located in Bedford, Ohio, offering a dynamic work environment where quality and safety are paramount. With a strong commitment to employee growth, comprehensive benefits including generous paid time off, and a focus on wellbeing, Hikma empowers its team members to thrive both personally and professionally while contributing to the vital mission of providing essential medicines to millions.
Contact Details:
Hikma Pharmaceuticals USA Inc. Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Supervisor, Quality Assurance in Bedford
✨Tip Number 1
Network like a pro! Reach out to current or former employees at Hikma Pharmaceuticals on LinkedIn. A friendly chat can give us insider info and maybe even a referral!
✨Tip Number 2
Prepare for the interview by brushing up on your knowledge of quality assurance in the pharmaceutical industry. We want to show that we’re not just qualified, but genuinely passionate about ensuring high-quality medicines.
✨Tip Number 3
Practice common interview questions with a friend or in front of the mirror. We need to nail our responses, especially when it comes to our leadership experience and problem-solving skills.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure our application gets seen by the right people. Plus, it shows we’re serious about joining the team at Hikma.
We think you need these skills to ace Supervisor, Quality Assurance in Bedford
Some tips for your application 🫡
Tailor Your Application:Make sure to customise your CV and cover letter to highlight your relevant experience in Quality Assurance. We want to see how your skills align with the job description, so don’t hold back on showcasing your expertise!
Showcase Your Leadership Skills:Since this role involves supervising others, it’s crucial to demonstrate your leadership abilities. Share examples of how you've led teams or projects in the past, and how you’ve contributed to quality improvements.
Be Clear and Concise:When writing your application, keep it straightforward and to the point. We appreciate clarity, so avoid jargon and make sure your key achievements stand out. This will help us quickly see why you’re a great fit!
Apply Through Our Website:We encourage you to submit your application directly through our website. It’s the best way for us to receive your details and ensures you’re considered for the role. Plus, it’s super easy!
How to prepare for a job interview at Hikma Pharmaceuticals USA Inc.
✨Know Your Quality Assurance Basics
Make sure you brush up on your knowledge of quality assurance principles, especially in the pharmaceutical industry. Understand the key regulations and standards that Hikma adheres to, as this will show your commitment and expertise during the interview.
✨Showcase Your Leadership Skills
As a Supervisor, you'll need to demonstrate your leadership abilities. Prepare examples of how you've successfully led teams or projects in the past, particularly in quality assurance or production settings. This will help you stand out as a candidate who can manage and inspire others.
✨Prepare for Scenario-Based Questions
Expect questions that ask how you would handle specific situations related to quality assurance, such as dealing with batch discrepancies or leading audits. Think through potential scenarios and formulate your responses to highlight your problem-solving skills and decision-making process.
✨Ask Insightful Questions
At the end of the interview, have a few thoughtful questions ready about Hikma's quality assurance processes or future projects. This shows your genuine interest in the role and helps you assess if the company is the right fit for you.
