International Graduate - Quality

Schott North America; South Lebanon Township (PA); Hybrid; USD 60,000 - 80,000; Full time

Benefits offered by this job

Flexible working hours

401(k) plan

Medical, dental, and vision coverage

Tuition reimbursement

Paid vacation days

Job summary

Schott North America is seeking a qualified candidate for a rotational development position focused on Quality Assurance and Quality Control processes. The role offers exposure to various departments and opportunities to lead improvement projects in a regulated manufacturing environment.

Ideal candidates possess a degree in a related field and a strong interest in the pharmaceutical industry. Additional benefits include flexible work hours and corporate pension plans.

Qualifications

• Up to 5 years of professional experience including internships or co-ops.
• Strong interest in Quality and pharmaceutical manufacturing.
• Flexibility to work in different departments and locations.

Responsibilities

• Participate in structured job rotations across Quality and cross-functional departments.
• Identify process improvement opportunities during departmental rotations.
• Support Quality activities in compliance with cGMP and ISO standards.
• Complete an international project assignment at another SCHOTT site.

Skills

Analytical skills

Problem-solving

Continuous improvement mindset

Communication skills

Time management

Education

Bachelor's or Master's degree in Quality, Engineering, Life Sciences, Chemistry, Biotechnology, Pharmacy or related

Tools

MS Office

SAP or similar systems experience

Job description

About us

Human health matters. SCHOTT Pharma designs science-based solutions to ensure medications are safe and easy to use globally. A team of 4,700 people from over 60 nations contributes to global healthcare. With 17 sites worldwide, the company is headquartered in Mainz, Germany, listed on the Frankfurt Stock Exchange, and committed to sustainable development for society and the environment.

Your Contribution

Rotational Development & Learning

• Participate in structured job rotations across Quality and selected cross‑functional departments.


• Gain hands‑on exposure to Quality Assurance, Quality Control, and Quality Systems processes within a regulated GMP manufacturing environment.


• Complete required technical, compliance, and professional development trainings.

Rotational Improvement Projects

• During each departmental rotation (1–2 months), identify opportunities for process, quality, compliance, or efficiency improvement.


• Develop a structured improvement project aligned with department objectives, Quality standards, and site KPIs.


• Apply basic continuous improvement, root cause analysis, data analysis, and problem‑solving methodologies.


• Prepare and deliver a formal presentation at the end of each rotation summarizing:




• Project objective and scope


• Analysis and methodology


• Results achieved


• Lessons learned and recommendations




• Document project outcomes and support knowledge sharing across departments.

Quality & Operational Support

• Support Quality activities in compliance with cGMP, ISO standards, and internal policies and procedures.


• Assist with documentation review, deviation investigations, risk assessments, CAPA activities, and change management initiatives.


• Participate in internal audits, inspections, and customer or regulatory interactions under supervision.


• Support maintenance and continuous improvement of the Quality Management System.

International & Cross‑Site Exposure

• Complete at least one international assignment or project at another SCHOTT site.


• Participate in benchmarking activities and exchange of best practices with global teams.


• Collaborate effectively within multicultural and cross‑functional environments.

General Responsibilities

• Prepare reports, presentations, and documentation for leadership review.


• Participate in meetings, workshops, and program evaluations.


• Follow all Company policies, procedures, EHS requirements, and safety protocols.


• Perform additional duties as assigned to support business and Quality objectives.

Your Profile

• Bachelor's or Master's degree in Quality, Engineering, Life Sciences, Chemistry, Biotechnology, Pharmacy, or a related technical discipline.


• Up to 5 years of professional experience (including internships, co‑ops, or trainee programs).


• Strong interest in Quality, pharmaceutical manufacturing, and regulated industries.


• Willingness and flexibility to work in different departments and locations, including international assignments.

Core Competencies

• Strong analytical and problem‑solving skills.


• Continuous improvement mindset.


• Basic knowledge or strong interest in cGMP, ISO standards, and Quality Management Systems.


• Project execution and time‑management skills.


• Ability to prepare and deliver clear, structured presentations.


• Strong verbal and written communication skills in English.


• Ability to work effectively in cross‑functional and multicultural teams.


• Proficiency in MS Office; SAP or similar systems experience is a plus.


• Learning agility, adaptability, and accountability.

Benefits

Schott offers a range of benefits including active health management through flexible working hours and hybrid work options, corporate pension plans, and additional benefits like 401(k) plan, medical, dental and vision coverage, tuition reimbursement, paid vacation days, holidays and sick time.

EEO Statement

At SCHOTT, it's your personality that counts - not your gender, your identity, or origin.