Analytical Lab Analyst (Waterford, IRL, IE)

<p style="text-align:center"><span style="text-decoration:underline"><strong>This is a hybrid position requiring the team member to be onsite a minimum of 3 days per week</strong></span></p> <p style="text-align:center"><span style="text-decoration:underline"><strong> No relocation is provided for this opportunity</strong></span></p> <p> </p> <p><span style="text-decoration:underline"><strong>Who We Are:</strong></span></p> <p>At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future?  </p> <p>There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families.</p> <p>We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.</p><div><div style="padding:10.0px 0.0px;border:1.0px solid transparent"><div style="font-size:16.0px;word-wrap:break-word"><H2 style="font-size:1.0em;margin:0.0px"><b>What We Offer</b></H2> </div><div><div>Global Career Opportunities: With facilities across North America, Europe, and Asia-Pacific, employees have opportunities for international exposure and cross-functional collaboration.</div><div>Inclusive &amp; Collaborative Culture: A global workforce that values diversity, equity, and inclusion—where all voices are heard and respected in a supportive environment.</div><div>Recognition &amp; Rewards: Performance-based bonuses, service recognition, and employee appreciation initiatives celebrate dedication and impact.</div></div></div><div style="padding:10.0px 0.0px;border:1.0px solid transparent"><div style="font-size:16.0px;word-wrap:break-word"><H4 style="font-size:1.0em;margin:0.0px"><b>Job Summary</b></H4> </div><div><p style="text-align:justify;margin:0.0cm;font-size:11.0pt;font-family:Arial, sans-serif"><span style="font-size:12.0pt;font-family:arial, helvetica, sans-serif">In this role, you are responsible for executing testing for both internal and external customers in a cGMP environment, including drug product testing.</span></p></div></div><div style="padding:10.0px 0.0px;border:1.0px solid transparent"><div style="font-size:16.0px;word-wrap:break-word"><H2 style="font-size:1.0em;margin:0.0px"><b>Essential Duties and Responsibilities</b></H2> </div><div><ul> <li>An expert in basic established techniques, equipment, and/or test methods while following standard operating procedures (SOPs).</li> <li>Experience is High Performance Liquid Chromatography (HPLC) and associated analytical techniques.</li> <li>Proficient with complicated techniques, equipment, data gathering and/or test methods.</li> <li>Collaborate and in some cases lead, evaluation of equipment and vendor discussions</li> <li>Liaise with other WSS sites to ensure consistency in testing and methodology</li> <li>Ensure AIQs for all WSS instruments are completed in a timely manner.</li> <li>Participate in all development, transfer, analysis of customer works as required.  </li> <li>Independently complete projects from initiation through completion.</li> <li>Actively participate in and complete all appropriate training tasks in a timely manner.</li> <li>Provide training on established techniques and/or test methods.</li> <li>Assist and participate with audits as required.</li> <li>Ensure metrology tasks for all WSS instruments are completed in a timely manner.</li> <li>Develop/Assist in lab study design and in study plans and protocols and methods.</li> <li>Assist in implementation of new methods, validations, and technologies as required.</li> <li>Liaise with vendors, clients and inter-departments as required.</li> <li>Author work instructions, SOPs, validations, technical reports, protocols and qualification documentation.</li> <li>Ensure documentation is consistent across WSS functions.</li> <li>Lead and/or participate in and complete simple lab investigations, OOS, Deviations, LIRs and CAPAs as required.</li> <li>Be efficient in the required laboratory software &amp; critical systems to perform the day-to-day required activities.</li> <li>Meet individual and departmental goals and metrics.</li> <li>Make rational and sound decisions at an individual level.</li> <li>Adhere to established laboratory safety procedures.</li> <li>Weekly and monthly laboratory clean routines.</li> <li>Follow required cGMP regulations and internal QA procedures.</li> <li>Possess ability to work independently and as part of a team with self-motivation, adaptability, and a positive attitude.</li> <li>Willingness to learn and apply new analytical techniques.</li> <li>Act in accordance with the company’s Guiding Principles and adherence to the corporate Code of Conduct</li> <li>Compliance to all local sites: Environmental, Health and Safety regulations and contributions to improvement of safety in the laboratory.</li> <li>Compliance with all local company policies, procedures and corporate policies.</li> <li>Other duties as assigned.</li> </ul></div></div><div style="padding:10.0px 0.0px;border:1.0px solid transparent"><div style="font-size:16.0px;word-wrap:break-word"><H2 style="font-size:1.0em;margin:0.0px"><b>Basic Qualifications</b></H2> </div><div><ul> <li style="font-size:12.0pt;font-family:arial, helvetica, sans-serif"><span style="font-size:12.0pt;font-family:arial, helvetica, sans-serif">Degree in chemistry, pharmacy or related scientific discipline. </span></li> <li style="font-family:arial, helvetica, sans-serif;font-size:12.0pt"><span style="font-family:arial, helvetica, sans-serif;font-size:12.0pt">Minimum 3 yeras  of relevant  experience in a pharmaceutical, pharmaceutical packaging or medical device / delivery systems company and cGMP environment. </span></li> <li style="font-family:arial, helvetica, sans-serif;font-size:12.0pt"><span style="font-family:arial, helvetica, sans-serif;font-size:12.0pt">HPLC experience is essential.</span></li> </ul></div></div><div style="padding:10.0px 0.0px;border:1.0px solid transparent"><div style="font-size:16.0px;word-wrap:break-word"><H2 style="font-size:1.0em;margin:0.0px"><b>Preferred Knowledge, Skills and Abilities</b></H2> </div><div><ul> <li style="text-align:justify;font-size:12.0pt;font-family:arial, helvetica, sans-serif"><span style="font-size:12.0pt;font-family:arial, helvetica, sans-serif">Able to be aware of all relevant standard operating procedures as per company policy as they are related to the position covered by this Job Description.</span></li> <li style="text-align:justify;font-size:12.0pt;font-family:arial, helvetica, sans-serif"><span style="font-size:12.0pt;font-family:arial, helvetica, sans-serif;color:black">Experience is High Performance Liquid Chromatography (HPLC)</span></li> <li style="text-align:justify;font-size:12.0pt;font-family:arial, helvetica, sans-serif"><span style="font-size:12.0pt;font-family:arial, helvetica, sans-serif">Experience with FDA, HPRA, ISO &amp; corporate audits.</span></li> <li style="text-align:justify;font-size:12.0pt;font-family:arial, helvetica, sans-serif"><span style="font-size:12.0pt;font-family:arial, helvetica, sans-serif">Support and contribute to Lean Sigma programs and activities towards delivery of the set target <span style="color:white"> #LI-NJ1 #LI-Hybrid</span></span></li> </ul></div></div><div style="padding:10.0px 0.0px;border:1.0px solid transparent"><div style="font-size:16.0px;word-wrap:break-word"><H2 style="font-size:1.0em;margin:0.0px"><b>Travel Requirements</b></H2> </div><div><div>None: No travel required</div></div></div></div><p><strong>Pay Transparency:</strong></p> <p>The annual base salary range for this position is €44,968.00 - €57,232.00. Total target compensation is determined using objective and gender-neutral criteria, including relevant experience, qualifications, skills, market benchmarks, geographic location, and the scope and responsibilities of the role.</p> <p>This position may be eligible for variable compensation and other incentive programs in accordance with the terms of the applicable plans within the country of employment. In addition, team members are eligible to participate in the company’s benefits and total rewards programs applicable to their location and employment status.</p> <p> </p> <p> </p> <p>West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status.  If you have a special need that requires accommodation in order to apply to West, please send an email to <a href="mailto:Apply.Accommodation@westpharma.com">Apply.Accommodation@westpharma.com</a>.  Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening.</p>