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Pharmaceutical Site Manager - job 1 of 2

Company Description

The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

If you’re looking for a rewarding career, a place to call home, apply with us today!  

Job Description

Position Requirements:

  • Provide role model leadership and foster morale and teamwork
  • Foster positive client relations by interfacing effectively with clients and create a superlative service culture.
  • Track metrics and ensure that the team is meeting productivity and quality standards.
  • Ensure performance standards are met.
  • Ensure adherence to highest quality and efficiency standards in laboratory operations.
  • Provide technical oversight with large and small molecule testing, GMP operations, technical support, and early phase research, as needed.
  • Facilitate employee meetings.
  • Oversee the performance management and development of staff.
  • Develop strong leadership team to support employees and clients. 

Qualifications

The ideal candidate would possess :

  • Excellent role model leadership and coaching skills
  • Relevant pharmaceutical GMP, GLP, and GRP industry experience
  • Proven success in leading and inspiring technical teams and developing leaders
  • Strong scientific, computer, and organizational skills
  • Excellent communication (oral and written) and attention to detail
  • Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
  • Strong emotional intelligence, self awareness, self assurance, adaptability, interpersonal skills, and openness to others ideas and input.
  • High energy and positive approach to situations and interactions.
  • Experience in recruiting highly preferred

Basic Minimum Qualifications :

  • BS/MS/PhD in chemistry, biology, biochemistry, microbiology or other related degree concentration, or equivalent directly-related experience
  • At least two years laboratory experience within the pharmaceutical industry
  • At least two years supervisory experience
  • Authorization to work in the United States indefinitely without restriction or sponsorship

Additional Information

Position is Full Time, Monday-Friday with overtime as needed. Candidates currently living within a commutable distance of West Point, PA are encouraged to apply.

  • Excellent full-time benefits including comprehensive medical coverage, dental, and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays
  • Eligibility for potential yearly Bonus & Merit-Based Pay Increases

Eurofins USA PSS Insourcing Solutions is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

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Average salary estimate

$85000 / YEARLY (est.)
min
max
$70000K
$100000K

If an employer mentions a salary or salary range on their job, we display it as an "Employer Estimate". If a job has no salary data, Rise displays an estimate if available.

What You Should Know About Pharmaceutical Site Manager, Eurofins

Are you ready to lead a team and make a substantial impact in the biopharmaceutical industry? As a Pharmaceutical Site Manager at Eurofins in West Point, PA, you will be at the forefront of ensuring that our laboratory operations meet the highest standards of quality and efficiency. In this role, you will provide exemplary leadership, fostering a collaborative environment where both team morale and client relations thrive. Your responsibilities will include tracking team productivity and quality metrics, delivering technical oversight on large and small molecule testing, and ensuring adherence to GMP operations. You’ll also facilitate employee meetings and oversee the performance management and development of your staff. Eurofins values emotional intelligence and a positive attitude, qualities that you will exemplify as you inspire your team. We are looking for someone with a strong scientific background—ideally with a BS/MS/PhD in a relevant field—and at least two years of supervisory experience in the pharmaceutical sector. If you are self-motivated, adaptable, and passionate about growing in an organization that invests in its employees, don’t hesitate to apply for this full-time position today. Join us at Eurofins to make life and our environment safer, healthier, and more sustainable, while enjoying competitive benefits and a supportive work culture.

Frequently Asked Questions (FAQs) for Pharmaceutical Site Manager Role at Eurofins
What responsibilities does a Pharmaceutical Site Manager at Eurofins include?

A Pharmaceutical Site Manager at Eurofins is responsible for providing role model leadership, fostering teamwork and morale among staff, tracking productivity and quality metrics, and ensuring that laboratory operations adhere to the highest efficiency and quality standards. This position also involves developing a strong leadership team to support both employees and clients.

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What qualifications are required for the Pharmaceutical Site Manager position at Eurofins?

To qualify for the Pharmaceutical Site Manager role at Eurofins, an ideal candidate should possess a BS/MS/PhD in chemistry, biology, biochemistry, or a related field, along with at least two years of laboratory experience within the pharmaceutical industry and two years of supervisory experience. Strong leadership, communication, and organizational skills are essential.

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What is the work schedule for the Pharmaceutical Site Manager role at Eurofins?

The Pharmaceutical Site Manager role at Eurofins is a full-time position working Monday to Friday, with overtime as required. Candidates should be flexible and prepared to work additional hours when needed to meet project deadlines and operational demands.

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How does Eurofins support the professional growth of its Pharmaceutical Site Managers?

Eurofins is dedicated to the professional development of its employees by providing the necessary tools, resources, and support for growth within the biopharmaceutical industry. This includes opportunities for training, mentorship, and leadership development to help employees climb the career ladder.

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What benefits can a Pharmaceutical Site Manager expect at Eurofins?

As a Pharmaceutical Site Manager at Eurofins, you can look forward to an excellent benefits package that includes comprehensive medical coverage, dental and vision options, life and disability insurance, a 401(k) plan with company match, paid vacation and holidays, and eligibility for potential yearly bonuses and merit-based pay increases.

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Common Interview Questions for Pharmaceutical Site Manager
Can you describe your leadership style as a Pharmaceutical Site Manager?

It's important to convey a leadership style that promotes collaboration and team morale. You might discuss how you lead by example, encourage open communication, and inspire your team to achieve goals collectively.

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How do you ensure quality and efficiency standards are met in laboratory operations?

Candidates should emphasize their familiarity with quality assurance protocols, how they track metrics, and the importance of continuous training and performance reviews to meet laboratory standards.

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What experience do you have with GMP operations?

Be prepared to discuss your direct experiences working within GMP environments, including specific roles you’ve held, challenges you faced, and how you addressed them while adhering to regulations.

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How do you handle conflicts or difficult situations among team members?

Demonstrating emotional intelligence is key; explain your approach to resolving conflicts by fostering open dialogue, understanding different perspectives, and promoting a collaborative working environment.

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What strategies do you apply to facilitate effective client relations?

Discuss how you prioritize communication, feedback, and building trust with clients to ensure their needs are met and they feel valued as partners.

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How do you track and measure team productivity?

Describe the tools or methods you use to track productivity, such as performance dashboards or project management software, and stress how you analyze data to identify improvements.

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Can you share an example of how you've developed leadership in your team?

Provide a specific example where you mentored team members, helping them to acquire skills and take on leadership roles themselves, which speaks volumes about your own leadership experience.

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What do you consider to be the biggest challenges in the pharmaceutical industry today?

Be well-versed in current industry trends and challenges, such as regulatory changes, technology advancements, or supply chain issues, and be able to discuss how you would navigate these challenges.

Join Rise to see the full answer
How do you balance operational demands with employee development?

Discuss your approach on how you prioritize both maintaining operational excellence while also providing growth opportunities to your employees.

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What motivates you as a Pharmaceutical Site Manager?

Speak to your passion for the biopharmaceutical field, your desire to lead effective teams, and your commitment to quality and safety in laboratory practices, illustrating your motivations with personal anecdotes.

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Full-time, on-site
DATE POSTED
March 11, 2025

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