Jobs at Good Shepherd Services

This full-time New Grad Registered Nurse role is part of a year-long residency program at Methodist Hospital Texsan, designed to support the transition from student to professional nurse within the hospital's Rehab department. The position involves assessing patient conditions, administering medications, performing clinical procedures, and educating patients and families on care plans. The program offers a supportive environment with preceptorship, monthly educational sessions, and mentorship from experienced nurse leaders. The role is appealing due to the comprehensive training structure, opportunities for professional growth, and the hospital's recognition as a top workplace with advanced cardiac and orthopedic services. Some travel may be required for training purposes.

This full-time entry-level role is a New Grad Registered Nurse position within the Methodist Healthcare Residency Program at Methodist Hospital Texsan. The year-long program supports the transition from student to professional nurse through advanced clinical training in rehabilitation, monthly educational sessions, and preceptorship. Key responsibilities include assessing patient conditions, administering medications, performing medical procedures, and educating patients and families on care plans. The position is appealing due to its structured mentorship from experienced leaders, a supportive learning community, and access to comprehensive benefits including tuition assistance and retirement matching. The role is based on-site with occasional travel required for training.

This Legal Executive Assistant role supports the Lateral Recruiting department at Ropes & Gray, a top-ranked global law firm. The position serves as a strategic partner to industry-leading lawyers, managing complex calendars, coordinating international travel, and handling sensitive document production and inbox management. Key responsibilities include organizing high-level meetings across multiple time zones, maintaining strict confidentiality, and utilizing advanced Microsoft Office skills to streamline recruitment workflows. The role appeals to self-starters seeking a challenging environment with significant growth potential, offering a collegial culture, comprehensive professional development, and a hybrid work arrangement that balances on-site collaboration with flexibility.

This full-time New Graduate Registered Nurse role is part of a year-long residency program at Methodist Hospital Texsan, designed to support the transition from student to professional nurse. The position focuses on the Rehabilitation specialty and includes key responsibilities such as assessing patient conditions, administering medications, performing clinical procedures, and educating patients and families on care plans. The role offers a supportive environment with mentorship from experienced nurse leaders, hands-on simulations, and monthly educational sessions. The position is appealing due to the hospital's reputation as a premier cardiac and orthopedic center, its recognition as a Best Place to Work, and comprehensive benefits including tuition assistance and retirement matching. While primarily on-site, some travel may be required for training.

This full-time New Grad Registered Nurse Residency at Methodist Hospital Texsan is a year-long program designed to support the transition from student to professional nurse within the hospital's Rehab department. The role involves delivering patient-centered care, assessing patient conditions, administering medications, and educating patients and families while collaborating with medical teams. Key responsibilities include participating in advanced clinical training, monthly educational sessions, preceptorship, and evidence-based practice projects. The position is appealing due to its comprehensive mentorship from experienced nurse leaders, a supportive learning community, and access to extensive benefits including tuition assistance and retirement matching. The program offers opportunities for professional growth in a recognized cardiac and orthopedic facility, with some travel required for training.

This full-time teaching and coaching position combines classroom instruction with leading athletic programs across multiple middle school campuses. The role involves designing and implementing sports curricula that emphasize skill development, teamwork, and sportsmanship while ensuring strict adherence to state athletic league regulations. Key responsibilities include supervising practices and competitions, managing student eligibility and safety protocols, and maintaining open communication with parents and school staff. The position offers the opportunity to mentor young athletes in a collaborative educational environment, fostering community pride and student growth. Candidates must possess a valid teaching certification and significant high school coaching experience. The work arrangement includes both indoor classroom duties and outdoor field activities, requiring flexibility for irregular hours and frequent travel to district events.

The Clinical Research Associate II role at AbbVie supports the advancement of the company's drug pipeline through rigorous clinical research execution. The position serves as the primary liaison between the sponsor and investigative sites, ensuring trial conduct aligns with protocols, Good Clinical Practices, and regulatory standards. Key responsibilities include conducting site monitoring and training, managing patient recruitment strategies, performing risk assessments to safeguard data integrity, and mentoring junior team members. This position appeals to professionals seeking a collaborative environment that values scientific excellence and patient safety. The role offers opportunities for professional growth through global initiatives and emphasizes a customer-centric approach to building trusted partnerships with investigators.

The Packaging Supervisor role on the first shift oversees daily operations within the packaging department at Carl Buddig and Company, a leading meat manufacturer with a strong family-owned heritage. Key responsibilities include creating and adjusting production schedules, training and supervising staff, enforcing safety and quality standards, and maintaining accurate inventory and records. The position offers the appeal of working for an established company that values teamwork, innovation, and community impact. The role requires physical stamina in a cold, fast-paced environment and provides opportunities for professional growth within a supportive culture.

The Lead Clinical Research Associate role serves as a senior leader within Alira Health's global clinical team, providing oversight and mentorship to ensure high-quality trial execution. Key responsibilities include managing site monitoring visits, supervising junior Clinical Research Associates, ensuring regulatory compliance with GCP and ICH guidelines, and maintaining audit readiness for Investigator Site Files. This position appeals to experienced professionals seeking a collaborative culture driven by shared values of courage and inclusivity, offering opportunities for career growth through people management and strategic project involvement. The role requires significant travel, up to 85%, to support global site visits and foster cross-functional teamwork.

This six-month onsite contract role serves as the Contract Manufacturing Manager at an external pharmaceutical facility near Frankfort, Kentucky. The position involves acting as the primary on-site representative to oversee small molecule drug product manufacturing, including granulation, blending, compression, and coating. Key responsibilities include managing manufacturing exceptions, conducting risk assessments through FMEA, and ensuring timely production while maintaining strict Good Manufacturing Practices. The role appeals to professionals seeking to apply their technical expertise in a dynamic environment with opportunities for cross-functional collaboration across global teams. Candidates with seven to ten years of experience in quality or technical roles within the pharmaceutical industry are ideal for this position.

The Family Planning Research Assistant 1 role supports clinical and translational research projects within Yale's Division of Family Planning in the Department of Obstetrics, Gynecology, and Reproductive Sciences. Key responsibilities include recruiting study participants, obtaining informed consent, collecting physical measurements and biospecimens, and managing research data with strict adherence to ethical guidelines. The position offers a collaborative environment where the assistant works alongside principal investigators and trainees to advance reproductive health science. This opportunity is appealing for individuals seeking to develop expertise in clinical trials and data analysis while contributing to meaningful medical research. The role operates on a hybrid work model and requires a strong work ethic with the ability to perform self-directed tasks.

This full-time Downline Operator role on the second shift supports beverage manufacturing operations at Finlays Solutions. The position involves palletizing finished goods, managing packaging materials, and maintaining case coding and tray packing equipment. Key responsibilities include adhering to strict safety and Good Manufacturing Practices, performing routine machine maintenance, and ensuring accurate product documentation. The role appeals to individuals seeking a hands-on position within a global industry leader that values integrity, continuous improvement, and a collaborative team environment. The job requires physical stamina for lifting and standing in a dynamic warehouse setting with temperature fluctuations, while offering opportunities to contribute to high-quality production standards.

The Clinical/Health Care Research Nurse serves as a key coordinator within the Institute for Clinical and Translational Science, supporting the design and execution of clinical trials. Key responsibilities include screening and enrolling patients, obtaining informed consent, managing regulatory documentation, and assisting with data collection and budget administration. This role appeals to nursing professionals seeking to accelerate translational science and foster innovation in healthcare. The position offers a hybrid work arrangement within Iowa, combining on-campus and remote duties, and provides a comprehensive benefits package including retirement contributions and paid leave.

This six-month onsite role in Irving, Texas, serves as an entry-level quality assurance position within Abbott's manufacturing and testing operations. The technician supports production schedules by performing incoming dimensional and visual inspections on medical device components such as cable harnesses and printed circuit boards using hand tools and advanced measuring instruments. Key responsibilities include maintaining accurate GMP and GLP compliant records, accepting or rejecting supplier lots, and documenting non-conformances to support regulatory initiatives. The position appeals to candidates seeking to work in a global healthcare environment where quality and safety are paramount, offering exposure to FDA and ISO standards while contributing to life-changing medical breakthroughs.

This full-time Pharmacy Technician role within the clinical trials department supports the execution of regulated medical studies. The position involves maintaining organized study files, dispensing medications and devices, calculating dosages, and managing inventory to ensure patient safety. Key responsibilities include monitoring compliance with federal and state regulations, preparing for quality assurance audits, and coordinating with trial sites and sponsors to resolve protocol issues. The role offers a stable 40-hour work week with opportunities to contribute to medical advancements through rigorous adherence to good clinical practices. While primarily based on-site, the position may require some travel for study-related activities.

The Clinical Trial Monitor II role within the Clinical Trials Office at Dana-Farber Cancer Institute ensures research compliance with federal regulations and institutional policies. Key responsibilities include conducting remote data reviews and onsite monitoring visits to verify data accuracy, developing monitoring plans, and mentoring new team members. The position requires managing multiple projects simultaneously while promoting a culture of regulatory awareness. This opportunity appeals to professionals seeking to contribute to groundbreaking cancer research within an inclusive, mission-driven academic environment. The role is based in Boston with occasional travel required for onsite visits.

The Clinical Research Coordinator role at Huntsman Cancer Institute supports the Principal Investigator in managing the implementation and quality control of cancer research studies across the Intermountain West region. Key responsibilities include ensuring regulatory compliance with FDA and IRB guidelines, managing study budgets and participant enrollment, and coordinating all aspects of patient interactions from screening to informed consent. The position also involves supervising junior staff and maintaining detailed research documentation. This opportunity appeals to professionals seeking to contribute to a mission-driven organization dedicated to reducing the global cancer burden. The role offers a collaborative environment with opportunities for professional growth, requiring a blend of administrative precision and patient-centered care within a hybrid work setting.

This full-time Clinical Research Associate role is dedicated to a single sponsor and requires candidates to reside in the US near major hub airports in the Southeast, Northeast, Central, or West regions. The position involves performing site monitoring visits, including selection, initiation, and close-out, while ensuring adherence to Good Clinical Practice and international guidelines. Key responsibilities include managing subject recruitment plans, overseeing regulatory submissions and data integrity, and maintaining accurate Trial Master Files. The role offers the opportunity to work with a leading global provider of clinical research services, contributing to the development of innovative medical treatments. This position is travel-intensive, requiring approximately 65-70% nationwide travel to support diverse study sites.

The Production Associate role at Tennessee Foam supports manufacturing operations in Knoxville for diverse industries including medical and bedding. The position involves operating machinery in compliance with GMP and ISO13485 standards, maintaining a clean and safe work environment, and ensuring products meet strict customer specifications. Key responsibilities include troubleshooting equipment issues, adhering to standard operating procedures, and participating in ongoing training for professional development. This opportunity appeals to candidates seeking a dynamic, growth-oriented career within a global company that values innovation and strong team collaboration. The role offers a casual yet productive culture with access to comprehensive benefits and career advancement pathways, requiring no travel and based entirely on-site.

The Packaging Quality Supervisor role is a full-time position within the Quality department at a beverage facility in Rochester, NY. This leader oversees packaging quality functions, manages a team of analysts, and ensures compliance with FDA and TTB regulations. Key responsibilities include directing product safety testing, leading root cause investigations for quality issues, maintaining laboratory operations, and facilitating new product commercialization. The position offers a collaborative culture focused on continuous improvement and community involvement, supported by flexible scheduling, generous paid time off, and comprehensive benefits. While primarily based on-site, the role includes occasional travel to suppliers and customers for technical support and audits.

This full-time Packer role supports 80 Acres Farms' mission to revolutionize sustainable agriculture by packaging pesticide-free produce in advanced vertical farming facilities. The position involves operating packaging machinery, ensuring products meet strict specifications, and maintaining a sanitized work environment through rigorous cleaning and adherence to good manufacturing practices. Employees are responsible for lifting items up to 50 pounds and standing throughout shifts in temperature-controlled settings. The role appeals to individuals passionate about food sustainability and offers comprehensive benefits including immediate health coverage, paid time off, and a 401(k) match. The company provides extensive on-the-job training in a collaborative culture that values diversity and purpose-driven work across multiple locations.

This full-time role serves as a Press Floor B-Operator within the Press Department at the TPT Plant, focusing on third-shift production from 3:30pm to 5:30am. The position involves operating machinery to remove quality products, adhering to strict food safety and manufacturing standards, and maintaining high productivity levels to meet daily quotas. Key responsibilities include ensuring safe work practices, managing machine output, and performing necessary cleaning and product changeovers. The role appeals to individuals seeking a stable position within a collaborative team environment that values integrity, continuous improvement, and customer focus. While the work requires physical stamina for lifting and maneuvering heavy loads, it offers the opportunity to contribute directly to the company's mission of producing pet treats in a fast-paced setting.