Urwah Admin

Boehringer Ingelheim

<div></div><div><div><div><div><p>As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.
</p><p>The primary purpose of this position is to provide technical direction and supervision within the assigned packaging area in alignment with company policies and corporate business plans. This includes ensuring technical competence through the proper selection and training of the workforce, maintaining a safe workplace through effective training, and implementing and sustaining compliance with regulatory standards such as cGMP and OSHA.
</p><p>The role also manages the documentation process related to Packaging and labeling activities, such as batch records and equipment logbooks, while supporting the development of a continuous improvement culture within the team. Additionally, the position focuses on adopting new technologies, optimizing production processes to maintain cost efficiency, and fostering a technically skilled and safety-conscious workforce.
</p></div></div><div><div><h2 class="jobSectionHeader"><b>Duties &amp; Responsibilities
</b></h2></div><div><ul><li>Supervise personnel and activities in the assigned area in order to produce high quality product or results.
</li><li>This role is expected to work on the floor with the employees as needed.
</li><li>Troubleshoot production problems, document findings, and implement solutions to resolve problems.
</li><li>Keep updated and train personnel in scientific principles, time management,GMP's, technical requirements, and all other policies and regulations governing the production of assigned product.
</li><li>Communicate to management progress of the department, problems, employee actions, new ideas, and all other pertinent information.
</li><li>Administration of company policies and safety programs and understanding and enforcing terms of the union contract.
</li><li>Interface with other department Process Leaders and employees in a professional manner to coordinate the activities and issues.
</li><li>Requisition purchase of operating supplies and recommends purchase of new or replacement equipment.
</li><li>Make recommendations to hire/terminate personnel and discipline personnel as needed according to policies and procedures.
</li><li>Participate in and/or chair appropriate meetings and committees as assigned.
</li></ul><ul><li>Performs all Company business in accordance with all regulations (e.g., EEO, FDA, etc.) and Company policy and procedures. When violations are noted/observed they are to be immediately reported to management. Demonstrated high ethical and professional standards with all business contacts in order to maintain the Company's excellent reputation in the community.
</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>Requirements
</b></h2></div><div><ul><li>High School Diploma
</li><li>Bachelor's degree preferred with 2 years professional experience. 6 years relevant experience in lieu of degree. Experience must be inclusive of 1 year leadership experience.
</li><li>Demonstrated ability to train others and complete OJT assessments.
</li><li>Demonstrates the ability to follow systematic continuous improvement methodologies and the willingness to identify, define, and implement process improvements.
</li><li>Experience must be inclusive of managing and auditing master receipts, batch records and process order data within relevant SAP/ERP software systems.
</li><li>Experience with word processing, spreadsheets, and database management required.
</li><li>Must be detail oriented, able to work with minimal supervision and self-motivated to utilize resources to troubleshoot as needed.
</li><li>Ability to manage multiple on-going projects with aggressive deadlines.
</li><li>Strong proofreading skills along with excellent communication and written capabilities.
</li><li>Must be proficient in MS office applications such as Word, Excel, Outlook, etc.
</li><li>Experience in ERP inventory control system(s)is preferred but not necessary.
</li><li>Must be able to readily learn and quickly become proficient in all software applications utilized for packaging equipment and operations.
</li></ul><p><b>Eligibility Requirements:
</b></p><ul><li>Must be legally authorized to work in the United States without restriction.
</li><li>Must be willing to take a drug test and post-offer physical (if required)
</li><li>Must be 18 years of age or older
</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>Desired Skills, Experience and Abilities</b></h2></div></div></div></div><div></div>

Process Leader, Packaging

<div></div><div><div><div><div><p>As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.
</p><p>This position provides direction and supervision in their assigned Logistics area according to company policies and corporate business plans, providing technical competence through proper selection and training of the work force, ensuring a safe work place, implementing and maintaining compliance status (cGMP,OSHA) within the department. Manages the documentation for material management and the flowing in/out of the logistics floor including, but not limited to,equipment logbooks, order fulfillments, inventory counts, etc. Assist in developing a continuous improvement philosophy. Implement new technologies. Assist in maintaining the lowest cost of production possible.
</p></div></div><div><div><h2 class="jobSectionHeader"><b>Duties &amp; Responsibilities
</b></h2></div><div><ul><li>Supervise personnel to include communicating to management the status and/or progress of departmental concerns, issues, employee actions, new ideas, and all other relevant information to ensure success within the department.
</li><li>Hire, train, coach and develop personnel within the department in accordance with polices and procedures.
<br>
Coordinate the activities and schedules of the department. Discipline personnel as needed according to policies and procedures.
</li><li>Prepare and/or manage departmental budget and monitor departmental expenses and capital projects. Responsible for purchase of operating supplies to include recommendations for new or replacement equipment. Coordination of cycle counts in the Department to control inventory in production areas.
</li><li>Material management inbound or outbound depending on the logistics area and ensuring accuracy of all material documents.
</li><li>Create, review and approve relevant SOPs, Controlled Forms and other business function documents to support regulatory compliance, change controls and company driven initiatives.
</li><li>Manage and maintain tracking system for department key performance indicators. Provide data/metrics to Management regarding individual, equipment, production trends; provide recommendations to resolve errors.
</li><li>Manage and oversee analysis of logistics issues by identifying root causes, documenting findings, and implementing effective solutions to resolve problems. Coordinate efforts to investigate and address production process deviations, ensuring timely resolution and continuous improvement.
</li><li>Ensure compliance with cGMP, APHIS, OSHA, EPA, EU, and JP regulations pertaining to production process.
</li><li>Direct engagement in process execution including performing, supervising and supporting logistic process steps ensuring safe, compliant and reliable outcomes.
</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>Requirements
</b></h2></div><div><ul><li>High School Diploma. Bachelor's Degree in related business or scientific field preferred.
</li><li>In addition to Bachelor's degree, 2 years professional experience. 6 years relevant experience in lieu of degree. Experience must be inclusive of 1 year leadership experience.
</li><li>Demonstrated ability to train others and complete OJT assessments. Demonstrates the ability to follow systematic continuous improvement methodologies and the willingness to identify, define, and implement process improvements. Experience must be inclusive of managing and auditing master receipts, batch records and process order data within relevant SAP/ERP software systems. Experience with word processing, spreadsheets, and database management required.
</li>Must be detail oriented, able to work with minimal supervision and self-motivated to utilize resources to troubleshoot as needed. Ability to manage multiple on-going projects with aggressive deadlines. Strong proofreading skills along with excellent communication and written capabilities. Must be proficient in MS office applications such as Word, Excel, Outlook, etc. Experience in ERP inventory control system(s)is preferred but not necessary. Must be able to readily learn and quickly become proficient in all software applications utilized for packaging equipment and operations.<br>
<li>
</li></ul><p><br>
<b>Eligibility Requirements:
</b></p><ul><li>Must be legally authorized to work in the United States without restriction.
</li><li>Must be willing to take a drug test and post-offer physical (if required)
</li><li>Must be 18 years of age or older</li></ul></div></div></div></div>

Process Leader, Logistics

<div></div><div><div><div><div><p>The gBDS /Med Data/AI - Boehringer Ingelheim is seeking a postdoctoral research fellow to help leverage scientifically rigorous digital health technologies that accelerate clinical development across therapeutic areas.
</p><p>The fellow will drive innovation in digital endpoints, remote monitoring technologies, and multimodal data analytics to enhance multiple facets of clinical trials&mdash;from identifying and recruiting suitable patients to capturing meaningful real-world outcomes such as quality of life, functional capacity, and disease progression. This research-focused role emphasizes translating digital health innovations into, deployable solutions that improve trial outcomes by better understanding patients&rsquo; journeys in the real-world setting. Work will be anchored in Boehringer Ingelheim&rsquo;s core therapeutic areas &mdash; e.g. respiratory, cardiovascular-renal-metabolic, oncology, CNS &mdash; with digital measures selected/evaluated in the context of clinically meaningful endpoints for those disease areas.<br>
</p><p></p><p>As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies&acute; success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim&acute;s high regard for our employees.
</p></div></div><div><div><h2 class="jobSectionHeader"><b>Duties &amp; Responsibilities
</b></h2></div><div><ul><li>Under supervisor/s guidance, lead research focused on evaluating , testing, and deploying digital health technologies (wearables, sensors, smartphone apps, patient-reported outcomes) to accelerate clinical development as well as manuscript preparation and submissions
</li><li>Conduct statistical analysis of multimodal real-world behavioral data to assess associations with key clinical outcomes of interest (e.g., treatment response, disease progression, adherence, data quality, patient phenotypes/stratification, digital endpoint validation, quality of life)
<br>
</li><li>Proactively design and lead the development of reusable, reproducible data analysis pipelines for extracting quality metrics, features, and validated digital endpoints from multimodal clinical trial data
</li><li>Design and execute validation studies to establish the scientific rigor, reliability, and clinical meaningfulness of digital health measures for trial use (e.g., patient identification/screening, enrollment optimization, quality-of-life assessment, functional outcomes)
</li><li>Collaborate with interdisciplinary and cross-functional teams (clinical development, biostatistics, data science, clinical operations, regulatory affairs) to communicate and present research findings through presentations and scientific reports
</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>Requirements
</b></h2></div><div><ul><li>Ph.D. from an accredited institution earned before the start date at Boehringer Ingelheim. Preferred degree in a quantitative field such as biomedical engineering, statistics, computer science, electrical engineering, data science, or a related discipline
</li><li>Demonstrable proficiency in at least one scripting language (Python or R preferred) and experience writing reusable, version-controlled (Git), and well-documented code
</li><li>Demonstrated scientific experience in digital health research as evidenced by publications, presentations, or successful digital health project implementations
</li><li>Strong background in applied data science, signal processing, time-series analysis, and machine learning/statistics, preferably in healthcare or clinical research domains
</li><li>Experience analyzing temporal health-related data from digital health applications, wearable/smartphone sensors (e.g., accelerometer, activity, sleep, voice or other physiological/behavioral measures) is strongly preferred
</li><li>Familiarity with clinical outcome assessment (COA) frameworks and patient-centered measurement, including PRO, ClinRO, ObsRO, and PerfO categories; experience with ePRO/eCOA instruments or FDA PRO Guidance concepts is a plus
</li><li>Excellent interpersonal, communication, and presentation skills with the ability to work effectively in a dynamic, collaborative, and cross-functional environment
</li>Working knowledge of regulatory frameworks relevant to digital health technologies, including FDA DHT/SaMD guidance, ICH E6 (GCP), and digital endpoint evidentiary standards (e.g., V3+, BEST Resource, DDT qualification pathway); is a plus<br>
<li>
</li></ul><p></p><p><b>Eligibility Requirements </b>:<br>
</p><div></div><ul><li>Must be legally authorized to work in the United States without restriction.
</li><li>Must be willing to take a drug test and post-offer physical (if required).
</li><li>Must be 18 years of age or older.
</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>Compensation</b></h2></div><div><p><br>
</p><p></p><p>Duration: Two years
</p><p>Location: Remote (within US)</p></div></div></div></div>

Post Doctoral Medical Fellow - Digital Health, Clinical Development, Clinical Research

<div><p><b>We are IMETA<br>
</b></p><p></p><p>ROPU IMETA is a Regional Operating Unit consisting of 6 mid-sized Operating Units: India, Turkey, Southern Africa (South Africa &amp; Sub Sahara Africa) Northeast &amp; West Africa, Near East &amp; UAE, Saudi Arabia, Gulf &amp; East Africa (SAGEA).
<br>
IMETA is home to more than 47 nationalities. We are a myriad of color and culture and embracing this diversity is one of our greatest opportunities.
<br>
We are a powerhouse of talent, and we work together to ensure that we grow, nurture, and retain our talent. Uniting and working together is the key to our success<br>
</p><p></p><p><b>THE POSITION<br>
</b></p><p></p><p>We are looking for a Medical Sales Representative based in Egypt. This position will be responsible in effectively representing and promoting Boehringer Ingelheim (BI) core products to existing and potential customers, by presenting the benefits of BI products, with the objective of maximizing sales revenue and increasing market share. Key responsibilities in this role include offering innovative, tailored solutions to ensure long term presence of the CRM portfolio whilst adhering to company best practices. This position will be reporting to the district manager.<br>
</p><p></p><p><b>Tasks &amp; Responsibilities:<br>
</b></p><p></p><ul><li>Sales Planning:
</li></ul><p>Builds and executes an effective Sales Action Plan with the objective of maximizing business in assigned territories and to ensure achievement of sales and market share targets/objectives Monitors the sales development and performance of Boehringer Ingelheim CRM products<br>
</p><p></p><ul><li>Sales Execution:
</li></ul><p>Works closely with district Sales Manager in executing an effective Sales Action Plan with the objective of maximizing business in assigned districts to ensure achievement of district sales targets/objectives
</p><p>Plan and schedule daily visits with existing and potential customers to deliver the company's core product messages
</p><p>Record and monitor product sales and obtain feedback from existing customers on product performance and activity
</p><p>Secure a consistent and sustainable growth in sales and revenue by identifying and developing new market opportunities<br>
</p><p></p><ul><li>Stakeholder Management:
</li></ul><p>Build strong and long partnerships with all key stakeholders and ensure their full awareness of Boehringer Ingelheim product benefit.
</p><p>Propose customized partnership programs for existing and future customers that need to build productive relations between them and the company<br>
</p><p></p><p><b>Requirements:<br>
</b></p><p></p><p>Bachelor&rsquo;s degree
</p><p>Minimum of 2 years' experience in the Market
</p><p>Previous experience in Cardio, Renal, Metabolic therapeutic areas is a plus
</p><p>Excellent communication and presentation skills
</p><p>Ability to build and maintain relations with internal and external stakeholders.<br>
</p><p></p><p><b>What&rsquo;s Next?
</b></p><p>We are looking forward to receiving your application! We will then have a look at your profile. If we see a match, we will invite you for a screening interview.<br>
</p><p></p><p><b>Screening:
</b></p><p>In order to comply with applicable export control laws, Boehringer Ingelheim periodically screens business relations (including job applicants) against sanctioned party lists (&ldquo;SPL&rdquo;). These checks may be performed by Boehringer Ingelheim or by any of its Affiliates. You acknowledge that Boehringer Ingelheim and/or its Affiliates will screen you against SPL and that for this purpose your personal data may be processed in relevant databases, including databases of third-party vendors that perform SPL screening for or on behalf of Boehringer Ingelheim or its Affiliates which may be located or accessible outside the EU. Boehringer Ingelheim is committed to ensuring an adequate level of protection of your personal data.</p></div>

Medical Representative- Alexandria

<div>
 <strong>
  We are IMETA
  <br/>
  <br/>
 </strong>
 ROPU IMETA is a Regional Operating Unit consisting of 6 mid-sized Operating Units: India, Turkey, Southern Africa (South Africa &amp; Sub Sahara Africa) Northeast &amp; West Africa, Near East &amp; UAE, Saudi Arabia, Gulf &amp; East Africa (SAGEA).
 <br/>
 <br/>
 IMETA is home to more than 47 nationalities. We are a myriad of color and culture and embracing this diversity is one of our greatest opportunities.
 <br/>
 <br/>
 We are a powerhouse of talent, and we work together to ensure that we grow, nurture, and retain our talent. Uniting and working together is the key to our success
 <br/>
 <br/>
 <strong>
  THE POSITION
  <br/>
  <br/>
 </strong>
 We are looking for a Medical Sales Representative based in Egypt. This position will be responsible in effectively representing and promoting Boehringer Ingelheim (BI) core products to existing and potential customers, by presenting the benefits of BI products, with the objective of maximizing sales revenue and increasing market share. Key responsibilities in this role include offering innovative, tailored solutions to ensure long term presence of the CRM portfolio whilst adhering to company best practices. This position will be reporting to the district manager.
 <br/>
 <br/>
 <strong>
  Tasks &amp; Responsibilities:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Sales Planning:
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 Builds and executes an effective Sales Action Plan with the objective of maximizing business in assigned territories and to ensure achievement of sales and market share targets/objectives Monitors the sales development and performance of Boehringer Ingelheim CRM products
 <br/>
 <br/>
 <ul>
  <li>
   Sales Execution:
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 Works closely with district Sales Manager in executing an effective Sales Action Plan with the objective of maximizing business in assigned districts to ensure achievement of district sales targets/objectives
 <br/>
 <br/>
 Plan and schedule daily visits with existing and potential customers to deliver the company's core product messages
 <br/>
 <br/>
 Record and monitor product sales and obtain feedback from existing customers on product performance and activity
 <br/>
 <br/>
 Secure a consistent and sustainable growth in sales and revenue by identifying and developing new market opportunities
 <br/>
 <br/>
 <ul>
  <li>
   Stakeholder Management:
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 Build strong and long partnerships with all key stakeholders and ensure their full awareness of Boehringer Ingelheim product benefit.
 <br/>
 <br/>
 Propose customized partnership programs for existing and future customers that need to build productive relations between them and the company
 <br/>
 <br/>
 <strong>
  Requirements:
  <br/>
  <br/>
 </strong>
 Bachelor&rsquo;s degree
 <br/>
 <br/>
 <strong>
  Minimum Of 2 Years' Experience In The Market
  <br/>
  <br/>
 </strong>
 Previous experience in Cardio, Renal, Metabolic therapeutic areas is a plus
 <br/>
 <br/>
 Excellent communication and presentation skills
 <br/>
 <br/>
 Ability to build and maintain relations with internal and external stakeholders.
 <br/>
 <br/>
 <strong>
  What&rsquo;s Next?
  <br/>
  <br/>
 </strong>
 We are looking forward to receiving your application! We will then have a look at your profile. If we see a match, we will invite you for a screening interview.
 <br/>
 <br/>
 <strong>
  Screening:
  <br/>
  <br/>
 </strong>
 In order to comply with applicable export control laws, Boehringer Ingelheim periodically screens business relations (including job applicants) against sanctioned party lists (&ldquo;SPL&rdquo;). These checks may be performed by Boehringer Ingelheim or by any of its Affiliates. You acknowledge that Boehringer Ingelheim and/or its Affiliates will screen you against SPL and that for this purpose your personal data may be processed in relevant databases, including databases of third-party vendors that perform SPL screening for or on behalf of Boehringer Ingelheim or its Affiliates which may be located or accessible outside the EU. Boehringer Ingelheim is committed to ensuring an adequate level of protection of your personal data.
 <br/>
 <br/>
 Our Company
 <br/>
 <br/>
 <strong>
  Why Boehringer Ingelheim?
  <br/>
  <br/>
 </strong>
 With us, you can develop your own path in a company with a culture that knows our differences are our strengths - and break new ground in the drive to make millions of lives better.
 <br/>
 <br/>
 Here, your development is our priority. Supporting you to build a career as part of a workplace that is independent, authentic and bold, while tackling challenging work in a respectful and friendly environment where everyone is valued and welcomed.
 <br/>
 <br/>
 Alongside, you have access to programs and groups that ensure your health and wellbeing are looked after - as we make major investments to drive global accessibility to healthcare. By being part of a team that is constantly innovating, you'll be helping to transform lives for generations.
 <br/>
 <br/>
 Want to learn more? Visit https://www.boehringer-ingelheim.com
</div>


<div></div><div><div><div><div>This position manages all equipment, process, systems and product related validation activities, except GXP related computerized systems for both Pharmaceuticals and Vaccines at the site . The position is critical to the compliance effort for both pharmaceuticals and vaccines and is responsible for assuring compliance of validated systems, process, equipment to current cGMP, FDA, EU, USDA and BI corporate requirements.As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.
</div></div><div><div><h2 class="jobSectionHeader"><b>Duties &amp; Responsibilities
</b></h2></div><div><ul><li>Manages personnel, budgets and projects relating to systems, process, cleaning and equipment validation in GXP relevant areas such as Operations, R'D, Marketing at the facility.
</li><li>Maintains comprehensive electronic data base for tracking compliance and qualification status of all critical GXP relevant equipment, systems and processes.
</li><li>Identifies current trends in regulatory compliance for all validation procedures for equipment, systems and processes. Implements and updates the validation master plan (VMP) to assure compliance with regulatory and corporate requirements.
</li><li>Supports Product and Engineering Departments in the selection, review, acquisition, and upgrade of production equipment to assure future IQ/OQ/PQscan be performed on equipment sourced.
</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>Requirements
</b></h2></div><div><ul><li>Bachelor degreefrom an accredited institutionin a scientific, bioengineering, or relevant discipline required, and a minimum of ten (10) years GMP validation experience in a GMP OR regulated manufacturing or similar environment.
</li><li>In lieu of a degree, a minimum of fifteen (15) years GMP validation experience in a GMP OR regulated manufacturing or similar environment.
</li><li>Experience must be inclusive of at least three (3) years in a leadership role leading people and/or projects.
</li><li>Shares technical and compliance knowledge horizontally and vertically across the site.
</li><li>Ability to plan, schedule, organize, prioritize, and coordinate project activities.
</li><li>Ability to function in a leadership role and within cross-functional teams.
</li><li>Strong knowledge of statistics, data bases, and quality principles.
</li><li>Ability to analyze validation and production data to assess compliance with GMP requirements and/or troubleshoot compliance problems.
</li><li>Must be self motivated and of high integrity.
</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>Desired Skills, Experience and Abilities</b></h2></div></div></div></div><div></div>

Manager, Validation

<div></div><div><div><div><div>The basic purpose of this position is to provide administrative and technical direction in Biologics Production according to company policies and corporate business plans, to provide technical competence through proper selection and training of the staff and the workforce, to ensure a safe work place through proper training of staff and the work force to implement and maintain compliance status (cGMP, OSHA) within the department, to implement strategies to reduce cost of goods and improve existing production processes. The incumbent will represent their assigned interest to the business contacts (customers, suppliers, etc.) inside as well as outside BI and serves as a backup to the Director, Vaccine Production or direct supervisor in the event of their absence.As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies&acute; success. We realize that our strength and competitive advantage lie with our people. We support our employees in several ways to foster a healthy working environment, meaningful work, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim&acute;s high regard for our employees.
</div></div><div><div><h2 class="jobSectionHeader"><b>Duties &amp; Responsibilities
</b></h2></div><div><ul><li>Direct and supervise assigned areas in order to manufacture high quality biological products.
</li><li>Assist in coordinating the transfer of new products from Process Development into Production and in manufacturing qualifying/validation serials.
</li><li>Troubleshoot production problems, document findings, and implement solutions to resolve problems
</li><li>Train personnel in scientific principles, time management, GMPs, technical requirements, and all other policies and regulations governing the production of biological operations.
</li><li>Communicate to management progress of the department, problems, employee actions, new ideas, and all other pertinent information.
</li><li>Administration of company policies and safety programs.
</li><li>Interface with other department managers and employees in a professional manner to coordinate the activities and issues.
</li><li>Prepare annual departmental budget and monitor departmental expenses and capital projects.
</li><li>Complete annual review of all production outlines, special outlines, etc.
</li><li>Participate in and/or chair appropriate meetings and committees as assigned.
</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>Requirements
</b></h2></div><div><ul><li>BS in related discipline with minimum 4 years of experience in related field and minimum 2 years previous leadership experience required; minimum of 5 years&acute; experience preferred.
</li><li>Effective interpersonal skills with a diverse group of individuals at all organizational levels
</li><li>Proficiency in relevant computer software and programs associated with area.
</li><li>Excellent written and verbal communication skills
</li><li>Experience in biological production environment. Technical knowledge of biological production equipment and all biological operations necessary to produce high quality biological products. Excellent management, verbal and written communication, coaching and teamwork skills. Ability to lead teams to achieve results.
</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>Desired Skills, Experience and Abilities</b></h2></div></div></div></div><div></div>

Manager, Biological Production

Join Boehringer Ingelheim and explore 9   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

Boehringer Ingelheim

About Company

Process Leader, Packaging

Process Leader, Logistics

Post Doctoral Medical Fellow - Digital Health, Clinical Development, Clinical Research

Medical Representative- Alexandria

Medical Representative- Alexandria

Manager, Validation

Manager, Biological Production