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As directed by the supervisor and/or group leader perform functions to fulfill orders for shipment to customers. This may include but is not limited to customer service support, replenishment, cycle counting, picking, packing, and manifesting. Employee may be trained in any or all of the required disciplines depending on business needs. Employee must work all assigned hours and may also be required to perform other duties as directed by the supervisor and or group leader.
Hours - Sunday-Friday - 11:30pm-7:30am
Responsible for training all employees in the areas of picking, packing, shipping of domestic and international order processes in accordance with all related Standard Operating Procedures (SOP). Train all revisions to SOPs of related tasks as necessary. Additionally, responsibility could include training employees in the areas of replenishment, receiving, and putaway of product in accordance with SOPs as needed. This position will be required to periodically attend a Train-the-Trainer course. Employee must work all assigned hours and may also be required to perform other duties as directed.
Hours - Monday-Friday - 7:30am - 3:30pm
The Senior Quality Engineer will support manufacturing quality assurance in the manufacturing, packaging, product release, and related systems. The position supports new quality system/methodologies implementation, training, and problem solving, including leading non-conformance investigations, root cause analysis, and development of corrective and preventive actions.
This position will work directly with Manufacturing, Engineering, Quality Control, and other Senior Quality Engineers to provide sustaining quality and compliance leadership. It is responsible for trending key quality metrics to drive quality, continuous improvement, and efficiency.
The Regulatory Senior Manager handles regulatory development and post-approval/regulatory compliance for assigned products. Participates on the product development/life-cycle management team to provide regulatory guidance for assigned pharmaceutical Prescription products. Manages relevant regulatory strategy components and interactions with Regulatory Authorities for these products. May perform due diligence efforts on new product opportunities.
Leads the development of generic pharmaceutical products. Main area of focus would be topical (Skin and ocular), parenteral and liquid oral product development:
- Experimental design and laboratory troubleshooting
- Set-up, preparation and execution of R&D trials and cGMP activities
- Drafting, reviewing and approving stability protocols and reports
- Preparation of technical presentations
- Interpretation of data
- Internal and external communications with other operating functional groups (Quality, Regulatory, Stability, Supply Chain, Management, contract research organizations (CROs), and others
- Product transfers and scale-up activities
- Physical and chemical characterization of selected prototypes
- Set-up, preparation and execution of laboratory activities
- Preparation and execution of R&D and cGMP manufacturing activities
- Supervision of technician
- Development team composed of technicians and/or junior chemists (Chemists I-III)
- Performance evaluations of team members
- Scientific discussions/training
- Intellectual property opportunities
Documents laboratory work in compliance with company policies, government regulations. Provides general support to Formulation and Process Development Department. Supervise technicians. Provide leadership in laboratory maintenance activities.
The Principal System Engineer confirms Solta products meet functional system requirements, coordinates activities involved in system level specification, testing, and development for medical device products in the aesthetic space. The applicant must be a hands-on self-starter, who has the ability to work collaboratively with a multi-disciplinary product development team in accordance with the standards IEC 62304, IEC 62366, IEC 60601, and ISO 13485.
Perform tasks within full-scale production manufacturing operations, including routine assembly; or quality assurance and reliability testing following established methods and procedures. Operators are to be cross-trained and expected to perform any/all essential tasks within the production/manufacturing operations within the standard run time associated with each assembly. Use of basic hand tools.
Bausch Health Companies, Inc. is a diverse and decentralized pharmaceutical company that is committed to focusing on our key stakeholders while delivering consistently high performance. Our values provide the overall direction for our company, and provide us with the tools necessary to rise to any challenge by leveraging our collective hard work and effort along with our unwavering competitive spirit. These values help us set goals based on our organization’s potential and what we hope it will become.
Under limited supervision, the Ocular Specialty Representative markets and promotes a range of B&L proprietary and generic prescription eye care products to physicians in private practice.
This territory covers downtown Chicago
Bausch Health is a diverse and decentralized pharmaceutical company that is committed to focusing on our key stakeholders while delivering consistently high performance. Our values provide the overall direction for our company, and provide us with the tools necessary to rise to any challenge by leveraging our collective hard work and effort along with our unwavering competitive spirit. These values help us set goals based on our organization’s potential and what we hope it will become.
Ortho Dermatologics is one of the largest prescription dermatology companies in the world dedicated to helping patients in the treatment of a range of therapeutic areas including psoriasis, actinic keratosis, acne, atopic dermatitis, cold sores, athlete’s foot, nail fungus and other dermatoses. The Ortho Dermatologics portfolio includes several leading acne, anti-fungal anti-infective and psoriasis products.
Ortho-Dermatologics is looking for an accomplished, consistent and driven high performer with proven selling skills to join its fast growing sales organization. Individual will be responsible for establishing, promoting and maintaining a high level of sales of Dermatological products, working within an established territory and serving as a sales representative to dermatologists to provide them with disease product information, and superior customer service and support.
The site Quality leader is the Management Representative for the site, and has direct responsibility for the site Quality system and leadership of the site Quality organization. He/She will ensure that a site Quality Management System is established, implemented and maintained for product manufacturing, control, storage, and primary distribution processes in accordance with applicable US Federal Regulations, ISO 13485 standards, Bausch & Lomb Global Quality requirements and applicable country regulations, (i.e. Brazil, Canada, Japan, Australia, etc.) . He/She is a member of the site leadership team and, in partnership with the site operations leader, will sponsor a Quality and Compliance-focused culture which embraces Right First Time and Continuous Improvement expectations. Directs all technical and GMP aspects of plant activities. Interfaces with other top management personnel to set policy and to assure adherence to these, in addition to governmental standards. Responsible for the decision on acceptability and release of all Greenville products.