Director of Operations Employer Siegfried Location Pennsville, NJ Start date Sep 3, 2026 View more categories View less categories Discipline Manufacturing & Production , Operations Required Education Bachelors Degree Position Type Full time Apply now Save job Click to add the job to your shortlist You need to sign in or create an account to save a job. Send job Job Details "Expect to grow", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents. As a trusted and respected partner to the pharmaceutical industry, we uphold the highest standards in safety, quality and sustainability, while fostering a culture that empowers you to thrive. Join a rapidly expanding global company, where diverse perspectives and experiences come together in a collaborative environment. Here, you'll find a workplace that values both collective success and your individual contributions—offering long-term opportunities to grow and make an impact.

Your Role:

Purpose of Position:

Our site in Pennsville has been part of the Siegfried family since 1928 and has around 180 employees. It is our drug substance manufacturing site for the US market and provides spray drying operations globally, with focus on pilot and commercial manufacturing of drug substances (APIs) and related. In the past months, we have undertaken significant projects and implemented strategic initiatives aimed at unlocking the full potential of the site. Within this context, we are currently looking to fill the position of Director of Operations. In this role, you will be responsible for the overall management of manufacturing at the site, playing a pivotal role in the transformative growth of our Pennsville facility. Success in this role will require adaptability, resilience, and the ability to navigate through a dynamic environment, given the recent changes and ongoing optimization efforts. If you are seeking a new career challenge and envision yourself as a team player who proactively takes initiative and are willing to roll up your sleeves to make a difference every day alongside your team, then you are the right personality for us. This is a unique opportunity to lead and contribute to the success of a crucial site within our organization, where your leadership skills and strategic mindset will be instrumental in driving the site's success even in the face of evolving challenges. Your responsibilities As Director of Operations, you will lead our Managers of Wet Trains, Physical Operations and Cleaning Experts as well as be responsible for our team of Chemical and Physical Operations Operators (ca. 60 employees). You are a direct report to the Site Head at our site in Pennsville and you will be a member of our Site Leadership Team (SLT).

Your tasks:

• Ensure that all plant operations are conducted in accordance with applicable federal and state laws to promote the safety of the plant employees
• Cooperate closely with development to design processes that fit the manufacturing capabilities and ensure that all new production processes are safe and in compliance with all relevant environmental regulations
• Establish and drive a culture of "first time right" for all production activities
• Lead all current and new production activities through supervision and delegation to ensure that all production requirements are met, till the conclusion of the campaign
• Lead through management teams (shift supervisors and operations managers) a broad operations team with training, continuous improvement and operational excellence as key foundations
• Collaborate closely with Compliance to implement all process validations, equipment qualifications, and rework/reprocessing activities as well as review and approve any deviations or investigations associated with production
• Coach and develop teams to next levels and in turn ensure similar development of indirect reports. Define the succession plan for Operations.
• Identify and implement process improvements to benchmark and then improve cycle time, capacity, yield, labor utilization, efficiencies, process reliability, and production costs
• Coordinate all DEA activities to ensure that all CFR regulations are met.

Manage implementation and adherence to all applicable DOT, IATA, IMO, SHE, DEA and cGMP regulations

Your Profile:

Knowledge and experience: Engineering or Chemistry Degree 5+ years of experience in a similar leadership role in chemical synthesis type manufacturing preferably within the pharmaceutical or life science industries. 10+ years of work experience within the pharmaceutical or chemical manufacturing industry. A proven track record in applying structured problem solving approaches such as Lean and Six Sigma is key to support improvements and cultural change in the operational organization. Relevant experience in managing a unionized team is a plus.

Soft Skills:

Proven ability to lead and manage by example, coach, and motivate employees, clearly communicate job requirements and effectively manage the performance of the assigned tasks, with a "hands-on" approach. Ability to identify and analyze issues, providing solutions, and forward-thinking through solid problem-solving and a data based approach. Excellent written, verbal and listening communication skills with the ability to communicate and form relationships at all levels, from entry level to Executive Committee.

Your Benefits:

Competitive performance-based bonus Employee Share Matching Plan 401(k) Match Medical, Dental, and Vision Offerings Life, Sickness and Accident insurance, and Long-term disability Increased Voluntary Life Insurance (employee and family) (optional) The anticipated salary for this role will be between $158,000 - 197,000 Founded in 1873 in Zofingen, Switzerland, Siegfried has grown into a global network of 13 sites across three continents. With a team of more than 3,800 highly skilled professionals, we take the innovations of our pharmaceutical customers to industrial scale and manufacture safe drugs for patients worldwide. As a fully integrated CDMO, Siegfried is one of the few organizations today that can carry out the development and manufacturing of APIs and finished dosage forms under one roof. This unique combination of know-how and experience makes us the most trusted partner in the pharmaceutical industry. Share this job Facebook Twitter LinkedIn Apply now Send job Apply now Save job Click to add the job to your shortlist You need to sign in or create an account to save a job. Get job alerts Create a job alert and receive personalized job recommendations straight to your inbox. Create alert Similar jobs Sr. Specialist Manufacturing West Greenwich, Rhode Island Senior Associate Manufacturing Thousand Oaks, California Associate Director/Director - Quality Control, Gene Therapies Lebanon, Indiana